MouseBook Mouse Catalog

~~All~~Embryo only Sperm only Cre only Tet only

Strain Name	Gene/Allele Symbol	Chr	Phenotype	Availability
(beta)-globin (mu)MT <-/->			(mu)MT<-/-> produces IgM H-chains.	Order
B6J.129-Kcnj16<tm1Sj tu>/H	Kcnj16	11	Disrupted Kir 5.1 Potassium Channel. Phenotype not known at this point.	Order
101/H			Inbred strain.	Order
102/H			Wild type, inbred strain.	Order
10Bob			Affected mice head-bob, circle and walk backwards.	Order
129S9/SvEvH-Nodal<tm 1Rob>/H	Nodal<tm1Rob>	10	Heterozygote viable. Homozygote early developmental lethal (does not gastrulate).	Order
129P2/OlaHsd			The mice have yellow coats and late onset severe vacuolation in brain (700+ days).	Order
129P2/OlaHsd-Prnp<tm 2Edin>/H	Prnp<tm2Edin>	2	No expression of the Prnp gene. Abnormalities in synaptic transmission, circadian rhythm and sleep. Increased susceptability to oxidative stress and copper toxicity. Cellular phenotypes in T cell activation.	Order From EMMA
129S/SvEvNimrH			Inbred strain.	Order
129S9/SvEvH			Wildtype.	Order
129/terSv - TgN(Hbb- b) 83Clo/Ws	Tg(Hbb-b1)83Clo	UN	Reiterated transgene is detectable by DNA in situ hybridisation.	Order
129/terSv-TgN(Hbb-b1 )83Clo, Pax6<Sey/+>/Ws	Pax6<Sey>	2	Reiterated transgene is detectable by DNA in situ hybridisation.	Order From EMMA
129/terSv-TgN(Hbb-b1 )83Clo, Pax6<Sey/+>/Ws	Tg(Hbb-b1)83Clo	UN		Order From EMMA
129S9/SvEvH.B6-a/H	a	2	Black coat colour. The non-agouti locus from C57BL/6J has been bred to congenicity on a 129S9/SvEvH background. This stock is homozygous for non-agouti (a/a).	Order
129-Fgfr3<tm1.1Aomw> /Aomw	Fgfr3<tm1.1Aomw>	5	All homozygous males, some homozygous females and some heterozygous males develop an abnormal skull phenotype sometimes with malocclusion, and may be smaller in size. The phenotype is not fully penetrant. Refer to publication for further information: PMID:19086028.	Order From EMMA
A/JH			Inbred strain.	Order
A.129P2-Nat2<tm1Esim >/H	Nat2<tm1Esim>	8	No overt phenotype.	Order From EMMA
C3H101H-a<13H>/H	a<13H>	UN	(hair - colour) non-agouti-13-Harwell, umbrous effect.	Order
C3H101H-a<16H>a<l>/H	a<16H>	2	(coat colour) black back and pinna hairs and agouti belly and flanks. Homozygotes die prenatally.	Order
C3H101H-a<16H>a<l>/H	a<l>	2		Order
C3H101H-a<17H>/H	a<17H>	UN	(hair - colour) non-agouti-17-Harwell.	Order
C3H101H-a<18H>/H	a<18H>	2	Homozygotes are non-agouti with very dark pinna hairs. A/a<18H> looks wild-type. a/a<18H> look umbrous i.e. non-agouti with agouti hairs along side of body and on the belly.	Order From EMMA
C3H101H-a<19H>/H	a<19H>	UN	(hair - colour) non-agouti-19-Harwell, black pinna hairs.	Order
C3H101H-a<20H>/H	a<20H>	UN	(hair - colour) non-agouti-20-Harwell.	Order
C3H101H-a<da>/H	a<da>	2	(hair - colour) Non-agouti with dark agouti belly.	Order
C3H101H-a<t-2H>/H	a<t-2H>	2	(hair - colour) black and tan.	Order
C3H101H-a<tl>/H	a<tl>	UN	Resembles a<t> but there is no clear dividing line between black on the back and tan on the belly. Additionally, the tan colour is present on face spreading above the eyes.	Order
C3H101H-a<u>/H	a<u>	2	(hair - colour) agouti-umbrous.	Order
STOCK A<y>/H	A<y>	2	(hair - colour, eye - colour, size - obesity, sterile) heterozygotes all the hair pigment is yellow and the eyes are black; they usually become obese and sterile after the first few months.	Order
B6.Cg-Tg(ACTFLPe)920 5Dym/H	Tg(ACTFLPe)9205Dym	UN	No overt phenotype.	Order From EMMA
C3H101H-Ada<b>/H	Ada<b>	UN		Order
C3H101H-Ada<c>/H	Ada<c>	UN		Order
C3H101H-Ada<c>/H	Ada<a>	UN		Order
B6;129P2-Adamts1<tm1 Dgen>/H	Adamts1	16	No overt phenotype.	Order From EMMA
B6;129P2-Adamts2<tm1 Dgen>/H	Adamts2	11	No overt phenotype.	Order From EMMA
B6;129P2-Adcyap1r1<t m1Dgen>/H	Adcyap1r1	6	No visible phenotype.	Order From EMMA
129P2/OlaHsd-Fbxl3<G t(CB0226)Wtsi>/H	Fbxl3	14		Order
C3H.Cg-Fbxl3<Afh>/H	Fbxl3<Afh>	14	Identified in circadian rhythm screen. Mutants have a long circadian period 24.23hr (a) and 24.12hr (b).	Order From EMMA
Akt2<tm1Wtsi>	Akt2	7	None.	Order
Tg(DSPMKP3)Ox(Albert )				Order
Ananisi			An ENU-induced mutation causing heritable anti-nuclear antibodies with variable penetrance by 12-16 weeks of age. Lymphocyte populations appear grossly normal by flow cytometry.	Order From EMMA
Anaya			An ENU-induced mutation causing heritable anti-nuclear antibodies with variable penetrance by 12-16 weeks of age. Lymphocyte populations appear grossly normal by flow cytometry.	Order From EMMA
Andromeda			An ENU-induced mutation causing heritable anti-nuclear antibodies with variable penetrance by 12-16 weeks of age. Lymphocyte populations appear grossly normal by flow cytometry.	Order From EMMA
TgN(DSPMKP3)Ox(Angel a)				Order
Ann Boleyn	Anb	UN	Heterozygotes have polydactyly of the hind limbs. Homozygotes have polydactyly of all four limbs.	Order
TgN(DSPMKP3)Ox(Annek a)				Order
Antonia			An ENU-induced mutation causing heritable anti-nuclear antibodies and variable proliferative and membranous glomerulonephritis with partial dominant phenotype and penetrance by 12-16 weeks of age. Lymphocyte populations appear grossly normal by flow cytometry and immunoglobulin levels.	Order From EMMA
C57BL/6J-Apc<Min>/5H	Apc<Min>	18	Mice develop life-shortening intestinal polyposis.	Order From EMMA
C57BL/6J-Apc<Min>/2H	Apc<Min>	18	(adenoma - anaemia) multiple intestinal neoplasia.	Order From EMMA
ApoE/PAI-1	Apoe<tm1Bres>	7	Shortened life span.	Order From EMMA
ApoE/PLGN	Apoe<tm1Bres>	7	Rectal prolapse. Shortened life span in homozygotes.	Order From EMMA
apoE tPA	Apoe<tm1Bres>	7	None.	Order From EMMA
apoE tPA	Plat<tm1Mlg>	8	None.	Order From EMMA
apoE tTg	Apoe<tm1Bres>	7	None.	Order From EMMA
apoE tTg	Tgm2<tm1Gml>	2	None.	Order From EMMA
STOCK Ar<Tfm>/H	Ar<Tfm>	X	Hemizygous males are outwardly female in appearance but internally they have testes.	Order
Araf<tm1Mmc>	Araf<tm1Mmc>	X	Araf knockout mice litters are approximately one-third to half the size of their wildtype siblings from day 3 to pre weaning and so do not normally reach breeding age. However, placing them on supplementary diet or removing competition from other siblings, allows some to survive post weaning. Post-natal lethality and neurological and gastrointestinal defects in mice with targeted disruption of the A-raf protein Kinase gene.	Order
Araf<tm1Mmc>	Araf<tm1Mmc>	X	X-linked gene.	Order
Araf:Beta-geo				Order
Araf<tm1Mmc>	Araf<tm1Mmc>	X	Araf knockout mice litters are approximately one-third to half the size of their wildtype siblings from day 3 to pre weaning and so do not normally reach breeding age. However, placing them on supplementary diet or removing competition from other siblings, allows some to survive post weaning. Post-natal lethality and neurological and gastrointestinal defects in mice with targeted disruption of the A-raf protein Kinase gene.	Order
B6;129S4-Rhog<tm1Tnr >/H	Rhog<tm1Tnr>	7	Mild hyper reactivity of lymphocytes to antigen receptor engagement.	Order From EMMA
Ariel			Hind limb paralysis from day 12 in homozygotes.	Order
C3H101H-Atp7a<Mo-10H >/H	Atp7a<Mo-10H>	X	(hair - colour) mottled.	Order
C3H101H-Atp7a<Mo-11H >/H	Atp7a<Mo-11H>	X	(hair - colour) mottled.	Order
C3H101H-Atp7a<Mo-12H >/H	Atp7a<Mo-12H>	X	(hair - colour) mottled.	Order
C3H101H-Atp7a<Mo-13H >/H	Atp7a<Mo-13H>	X	(hair - colour) mottled.	Order
C3H101H-Atp7a<Mo-14H >/H	Atp7a<Mo-14H>	X	(hair - colour) mottled. Males do not survive.	Order
C3H101H-Atp7a<Mo-17H >/H	Atp7a<Mo-17H>	X	(hair - colour) mottled.	Order
Atp7a<Mo-18H>	Atp7a<Mo-18H>	UN	Mottled coat. Hemizygous males die in utero. The coat colour of females are typical Atp7a<Mo> but Atp7a<Mo-18H> has not been studied in depth.	Order
C3H101H-Atp7a<Mo-blo >/H	Atp7a<Mo-blo>	X	(hair colour) blotchy.	Order
C3H101H-Atp7a<Mo-ca> /H	Atp7a<Mo-ca>	X	(hair colour) Mottled candy.	Order
C3H101H-Atp7a<Mo-dp> /H	Atp7a<Mo-dp>	X	(hair - colour, gait, skeleton) mottled dappled.	Order
C3H101H-Atp7a<Mo-spt >/H	Atp7a<Mo-spot>	X	(hair - colour) mottled spot.	Order
C3H101H-Atp7a<Mo-to> /H	Atp7a<Mo-to>	X	(hair - colour) mottled tortoiseshell.	Order
C3H101H-Atp7a<Mo-vbr >/H	Atp7a<Mo-vbr>	X	(hair - colour, viable brindled.	Order
C3H;C-Pde6b<atrd1>/H	Pde6b<atrd1>	5	Eyes-slow onset retinal degeneration.	Order From EMMA
C3H;C-Pde6b<atrd2>/H	Pde6b<atrd2>	5	Slow onset retinal degeneration.	Order From EMMA
C3H;C-Pde6b<atrd3>/H	Pde6b<atrd3>	5	Eyes- slow onset retinal degeneration.	Order From EMMA
C3H;C-Pde6b<rd1-2H>/ H	Pde6b<rd1-2H>	5	Slow onset retinal degeneration.	Order From EMMA
C3H;C-Pde6b<rd1-3H>/ H	Pde6b<rd1-3H>	5	Slow onset retinal degeneration.	Order From EMMA
C3H;C-Pde6b<rd1-4H>/ H	Pde6b<rd1-4H>	5	Slow onset retinal degeneration.	Order From EMMA
B(Beta)DB<tm2Ked>	Dtnb	12	None observed.	Order
B10.L-Lsh	Slc11a1<r>	1		Order
B10ScSn.BXSB-(D1Mit3 -D1Mit320) Chr Y<BXSB/MpJ>/BjmjrH			Enhanced autoantibody spectrum and titre.	Order From EMMA
B10ScSn.BXSB-(D1Mit3 -D1Mit235) Chr Y<BXSB/MpJ>/BjmjrH			Enhanced autoantibody spectrum and titre.	Order From EMMA
B10ScSn.BXSB-(D1Mit1 23-D1Mit1000) Chr Y<BXSB/MpJ>/BjmjrH			Enhanced autoantibody spectrum and titre. Glomerulonephritis susceptibility.	Order From EMMA
B10ScSn.BXSB-(D1Mit2 35-D1Mit1000) Chr Y<BXSB/MpJ>/BjmjrH			Glomerulonephritis susceptibility.	Order From EMMA
B10ScSn.BXSB-(D1Mit3 03-D1Mit305) Chr Y<BXSB/MpJ>/BjmjrH			Glomerulonephritis susceptibility.	Order From EMMA
B10ScSn.BXSB-(D1Mit3 3-D1Mit223) Chr Y<BXSB/MpJ>/BjmjrH			ANA, 75% mortality, enhanced autoantibody titre, severe glomerulonephritis.	Order From EMMA
B6J.CBA-TgN(HDexon1) 61Gpb	Tg(HDexon1)61Gpb	UN	Huntington's disease, tremors, weight loss, movement disorders, died on average at 7 months old.	Order
B6.129-Igf1r<tm1.2Mh z>/Orl	Igf1r<tm1.2Mhz>	7	Live longer; resistant to oxidative stress.	Order
B6.Cg-Mir155<tm1.1Br d>Tyr<c-Brd>/H	Mir155<tm1.1Brd>	16	No visible phenotype is associated with this mutation but the mice do exhibit reduced lung airway remodelling & deficient B-cell, T-cell & dendritic cell function. This mutation is on a C57BL/6<c-/c-> background and is albino in appearance. The BIC mice (EMMA ID EM:02231) have been backcrossed at least 5 times to C57BL/6, thus making them suitable for bone marrow transplantation, without rejection, to any C57BL/6 mice, regardless of coat color.	Order From EMMA
B6.Cg-Mir155<tm1.1Br d>Tyr<c-Brd>/H	Tyr<c-Brd>	7		Order From EMMA
B6;D2-Tg(Sycp1-cre)4 Min/J	Tg(Sycp1-cre)4Min	UN	None given.	Order
B6CBA-Tg(HDexon1)61G pb	Tg(HDexon1)61Gpb	UN	Model for Huntington's disease, tremors, weight loss, movement disorders, die on average at 7 months old.	Order
BAC3			Normal.	Order
BALB/c			Albino.	Order
BALB/cOla			White coat colour.	Order
C.Cg-Il1rn<tm1Nick>/ Nick	Il1rn<tm1Nick>	2	Strain sporadically and independently develops rheumatoid-like arthritis, localised psoriasis-like lesions and patchy transmural destructive arteritis of the elastic vessels. Hygiene dependent (negative correlation). Different strain dependence of each disease. This strain, our SPF lab, 80% affected (each disease independently) at 200 days.	Order From EMMA
CBy.129-Rag2<tm1Fwa> /H	Rag2<tm1Fwa>	2	Chronic intestinal inflammation, colitis.	Order From EMMA
CBy.129-Cd44<tm1Ugu> Rag2<tm1Fwa>/H	Cd44<tm1Ugu>	2	Chronic intestinal inflammation, colitis.	Order From EMMA
CBy.129-Cd44<tm1Ugu> Rag2<tm1Fwa>/H	Rag2<tm1Fwa>	2	Chronic intestinal inflammation, colitis.	Order From EMMA
CBy.129-Cd44<tm2.1Ug u> Rag2<tm1Fwa>/H	Rag2<tm1Fwa>	2	Mice are homozygous for both Rag-/- and CD44v10-/- knockouts. Rag2-/-, no mature T and B cells. CD44v10-/-, strongly reduced symptoms in autoimmune diseases. Used in mouse models of experimental colitis.	Order From EMMA
CBy.129-Cd44<tm2.1Ug u> Rag2<tm1Fwa>/H	Cd44	2		Order From EMMA
CBy.129-Cd44<tm1.1Ug u> Rag2<tm1Fwa>/H	Cd44<tm1.1Ugu>	2	Rag2-/-: no mature T and B cells. CD44v6v7-/-: strongly reduced symptoms in autoimmune diseases.	Order From EMMA
CBy.129-Cd44<tm1.1Ug u> Rag2<tm1Fwa>/H	Rag2<tm1Fwa>	2		Order From EMMA
BALB/cPye				Order
C3H101H A/A<w>-Bbn/H	Bbn	UN	Affected animals are deaf and exhibit headbobbing and circling behaviour.	Order From EMMA
C3H101H-Bhd/H	Bhd	X	(head - nose) broad-headed.	Order
BHV11			Abnormal craniofacial features.	Order From EMMA
BHV26			The alternation score suggest this line has a potential short term working memory deficit.	Order From EMMA
BHV31			High anxiety.	Order From EMMA
BHV32			Hyperactivity.	Order From EMMA
BHV43			Possible short-term working memory deficit indicated by reduced spontaneous alternation in the Y-maze.	Order From EMMA
BHV48	Rgs18	1	None apparent, in heterozygotes.	Order From EMMA
C3H.Cg-Trpc3<Mwk>/H	Trpc3<Mwk>	3	Staggering, ataxic with limited movement in back legs. Heterozygotes are usually small.	Order From EMMA
ABL			Inbred strain.	Order
C3H101H-Fras1<bl>/H	Fras1<bl>	5	(eye, feet, kidney, skin) blebbed.	Order From EMMA
C57BL/6J-blst/H	blst	UN	Spontaneous recessesive coat colour mutation - light grey coat colour.	Order From EMMA
C57BL/6J-Btnt/H	Btnt	UN	Tan coat colour on belly.	Order From EMMA
C3H;C-Snap25<Bdr>/H	Snap25<Bdr>	2	Poor sight. Blind drunk. Small at weaning. SHIRPA anomalies including reduced or absent visual placing and staggering gait. Homozygotes have not been identified.	Order From EMMA
C57BL/6J-Blite/H	Blite	UN	White with non-agouti patches. Some patches reverting to non-agouti are visible in a small number of offspring. Timed matings of heterozygous stock can yield oedematous embryos.	Order From EMMA
BLUFF			Fluffy coat, abnormal hair distribution and texture.	Order
C3H101H-Papss2<bm>/H	Papss2<bm>	19	(skeleton) dwarfism - cleft palate brachymorphic.	Order
BMD2			Low bone mineral density.	Order
Bmp5<se-19H>	Bmp5<se-19H>	UN	Short-ear.	Order
Bmp5<se-20H>	Bmp5<se-20H>	UN	Short-ear.	Order
Bmp6<tm1Rob>	Bmp6<tm1Rob>	13	Mice show no overt phenotype.	Order From EMMA
Bmp7<tm2Rob>	Bmp7<tm2Rob>	2	Homozygous embryonic lethal.	Order From EMMA
Bmp7<tm1Rob>	Bmp7<tm1Rob>	2	This strain is a null allele of BMP7 generated by replacing the BMP7 coding sequence by a neomycin cassette. BMP7 is required in the metanephric mesenchyme of the developing kidney to support maintenance of this cell population during organogenesis. Homozygous lethal at birth due to kidney agenesis.	Order From EMMA
Zic3<Bn>, Atp7a<Mo-b r>	Zic3<Bn>	X	(coat colour) mottled brindled, Bent tail.	Order
C3H101H-Nsdhl<Bpa-1H >	Nsdhl<Bpa-1H>	X	(skin, size, tail ) bare patches.	Order
C3H101H-Nsdhl<Bpa-3H >	Nsdhl<Bpa-3H>	X	(skin - skeleton) scarring on females at 4 days old. More females than males born and some have spine abnormalities. Bare patches are clearly visible at weaning.	Order
C3H101H-Nsdhl<Bpa-4H >	Nsdhl<Bpa-4H>	X	(skin - skeleton) phenotype classed at 8 days but are barely visible at weaning. More females than males are born and they are prone to spinal abnormalities.	Order
C3H101H-Nsdhl<Bpa-5H >	Nsdhl<Bpa-5H>	X	(skin - skeleton - size) phenotype classed at 8 days some are small at birth. More females than males born and they are prone to spinal abnormalities.	Order
C3H101H-Nsdhl<Bpa-6H >	Nsdhl<Bpa-6H>	X	(skin) bare patches classed at 4 days and are clearly visible at weaning.	Order
C3H101H-Nsdhl<Bpa8H> /H	Nsdhl<Bpa-8H>	X	Male lethal. Females are classified at 8 days by scarring on the skin, small at weaning. The adult females are striped.	Order From EMMA
C3H101H-Br/H	Br	17	(nose - mouth, kidneys - size) brachyrrine.	Order
Brd7<tm1aWtsi>	Brd7	8	None.	Order From EMMA
Brn3a Knockout	Pou4f1	14	Homozygote neonate lethality caused by lack of suckling due to defects in sensory and motor neurons.	Order
Brn3b Knockout	Pou4f2	8	Homozygotes are blind due to failure of the retinal ganglia to develop.	Order
B6NDen;B6N-Brpf1<tm1 a(EUCOMM)Wtsi>/H	Brpf1<tm1a(EUCOMM)Wt si>	6		Order From EMMA
C3H101H-Gsdma3<Bsk>/ H	Gsdma3<Bsk>	11	(skin, eyes) bareskin, corneal opacities.	Order
Bstk			(hair - colour) Affected individuals have a belly spot and light feet.	Order
bv	bv	5	Bronx Waltzer. Recessive mutant; hyperactivity, circling, headbobbing and deafness in the homozygote.	Order From EMMA
bv (Bronx Waltzer)	bv	5	Bronx Waltzer.	Order From EMMA
C.D2-vil6				Order
C3H-nr/H	nr	8	Homozygotes are smaller in size and have hyperactive ataxic behaviour.	Order
C3H/HeH				Order
C3H;C-Chd7<Todo>/H	Chd7<Todo>	4	Headweaving and circling in heterozygotes. Homozygotes die at mid gestation with vascular and brain defects.	Order From EMMA
C3H;C-Chd7<Edy>/H	Chd7<Edy>	4	Headweaving/circling.	Order From EMMA
C3H;C-Chd7<Dz>/H	Chd7<Dz>	4	Dizzy. Heterozygote animals are small at birth with slight kink in tail and exhibit head weaving and circling behaviour.	Order From EMMA
B6.Cg-Il1rn<tm1Nick> /Nick	Il1rn<tm1Nick>	2	Strain resistant to arthritis, arteritis and psoriasis (seen in BALB/c) but highly susceptible to undefined 'malaise' under conventional conditions.	Order From EMMA
B6.129P2-Fgfr3<tm1.1 Aomw>/Aomw	Fgfr3<tm1.1Aomw>	5	All homozygous males, some homozygous females and some heterozygous males develop an abnormal skull phenotype sometimes with malocclusion, and may be smaller in size. The phenotype is not fully penetrant.	Order From EMMA
C57BL/6-Lep<ob>/H	Lep<ob>	6		Order
B6CBF1-Tg(ATXN3*)84. 2Cce/H	Tg(ATXN3*)84.2Cce	UN	Slowly progressive cerebellar defecit from 4weeks of age; wide flattened gait, clasping of all 4 limbs, neuronal loss, gliosis & neuronal intranuclear inclusions present in the pons & cerebellum, peripheral nerve demyelination.	Order From EMMA
C57BL/6Apb-Ptprc<loc >/Apb	Ptprc<loc>	1	Decreased expression of CD45 on CD19+ B cells etc.	Order From EMMA
C57BL/6Apb-Zap70<mur >/Apb	Zap70<mur>	1	Reduced naïve CD4+ and CD8+ T cells which are hyperactivated, reduced CD4+ cells, defect in TCR signal transduction, impaired but not severe response to anti-TCR stimulation, T cell intrinsic defect, elevated serum levels of IgG2b.	Order From EMMA
C57BL/6J-A<vy>/H	A<vy>	2		Order
C57BL/6J-Krt25<Re>/H	Krt25<Re>	11		Order
C57BL/6J-Kitl<Sl-d>/ H	Kitl<Sl-d>	10		Order
C57BL/6J-Ucp1<m1H>/H	Ucp1<m1H>	8	Homozygotes are unable to thermoregulate.	Order
STOCK a<t>/H	a<t>	2	(hair - colour) the back is black and the belly cream or yellow.	Order
C57BL/Ola-Gpi1-s<c>, c/Ws	Gpi1<c>	7		Order From EMMA
B6.AK-Gpi1<a>/Ws	Gpi1<a>	7		Order From EMMA
C57bl/ws-TgN(Hbb-b1) 83Clo/ws	Tg(Hbb-b1)83Clo	UN	None expressed.	Order From EMMA
C57BR/cd			Hepatomas in 25% of males.	Order
C3H101H-Krt71<Ca-2H> /H	Ca<2H>	UN	(Coat - texture) caracul. Homozygotes are indistinguishable from heterozygotes. Both are fully fertile and viable. Vibrissae are curved, and hair is wavy from time of first appearance until about 4 weeks of age. After this time the waves disappear, but the hair has a plush-like look.	Order
Krt71<Ca-d>, Scn8a<m ed>	Scn8a<med>	15	(Coat - texture, motor end plate).	Order
Krt71<Ca-d>, Scn8a<m ed>	Krt71<Ca-d>	15	(Coat - texture, motor end plate).	Order
129P2/OlaHsd-Tpcn1<G t(XG716)Byg>/H	Tpcn1	5		Order
B6;129-Capn5<tm1Nde> /H	Capn5<tm1Nde>	7	None apparent.	Order From EMMA
TgN(UbiCFL)Ox(Calvin )				Order
Candy			Hyperglycaemia, glycosuria. Elevated plasma glucose at 16 weeks of age. Glucose also detected in the urine at 24 weeks of age.	Order From EMMA
Candy2			Elevated plasma glucose at 16 weeks of age. Glucose also detected in the urine at 24 weeks of age.	Order From EMMA
Candy3			Elevated plasma glucose at 16 weeks of age. Glucose also detected in the urine at 24 weeks of age.	Order From EMMA
Candy4			Elevated plasma glucose at 16 weeks of age. Glucose also detected in the urine at 24 weeks of age.	Order From EMMA
Candy5			Elevated plasma glucose and phosphate at 16 weeks of age. Glucose also detected in the urine at 24 weeks of age.	Order From EMMA
B6;129P2-Capn1<tm1Dg en>/H	Capn1	19	No overt phenotype	Order From EMMA
C3H.C-Casp3<I216F>/H	Casp3	8	Reduced apoptosis in homozygotes. Phenocopies Caspase 3 null alleles.	Order From EMMA
C3H-Cat2/H	Cat2	1	(eye - cataract) cataract-2 dominant cataract.	Order
C3H101H-Cryga<tol>/H	Cryga<tol>	1	Dominant cataract.	Order
C3H-Cat5<To2>/H	Cat5<To2>	10	(eye - cataract) cataract-5 dominant cataract.	Order
CBA-TgN(IL5) 1 GlX			Transgenic pups have high leucocyte counts and are readily identifiable by differential leucocyte counts.	Order From EMMA
CBA/CaH	Xic<a>	X		Order
Runx1t1<tm1Fc>	Runx1t1<tm1Fc>	4		Order
CCBAN3-2371				Order
CCBAN4-2513				Order
CCBAN4-2547				Order
B6;129P2-Ccr9<tm1Dge n>/H	Ccr9	9	None.	Order From EMMA
CD2/NPM-ALK			Mice develop tumours of haemopoietic organs within 2 years of age in approx. 10% of mice.	Order From EMMA
CD45R03			Under investigation: not severely immunocompromised.	Order
CD45RABC3			Under investigation, not severely immunocompromised; no obvious immunological dysfunction.	Order
CD45RB2			Under investigation: not severely immunocompromised.	Order
CD45RO-C817S			Severe defects in B and T cell differentiation and function.	Order
CD45RO9			Under investigation, not severely immunocompromised.	Order
CEMO_S2				Order
CEMO_S3				Order
CEMO_S5				Order
CHANGELING			Motor co-ordination problems & death before weaning age.	Order
TgN(UbiCFL)Ox(Chelse a)				Order
Chm	Tyr<c-ch>	7		Order
STOCK Oca2<p>Tyr<c-c h>Myo7a<sh1>Prss8<fr>/H	Oca2<p>	7		Order
	Prss8<fr>	7
	Tyr<c-ch>	7
	Myo7a<sh1>	7
C3H101H-Flt4<Chy>/H	Flt4<Chy>	11	Milky abdomen shortly after birth. (abdomen, feet) chylous ascites.	Order From EMMA
Chy-Ma like			(abdomen, feet) chylous ascites. Milky abdomen. Small at birth and weaning. May have low fertility. Some may have coat dilution or headbobbing.	Order
C3H101H-Chy2/H			(abdomen, feet , tail). Typical chylous phenotype of puffy feet, swollen tail. No knowledge of fate of homozygote.	Order
Chy5	Chy5<Ma1>	UN	milky abdomen.	Order
Chy6	Chy6<Ma2>	UN	milky abdomen.	Order
C3H101H-Chy7/H			(abdomen, feet) chylous ascites. Milky abdomen.	Order
CIRCA12			Identified in circadian rhythm screen. Has a reduced period lengthening response when subjected to constant light conditions.	Order
CIRCA2			Long activity under constant dark period.	Order
CIRCAD21				Order
B6.Cg-Cited2<L247P>/ H	Cited2	10	Although the amino acid change occurs in a highly conserved residue. The mutant is homozygous viable and fertile, with no detectable phenotype. In trans to the Knock-out allele, it is viable and phenotypically normal.	Order From EMMA
B6J.129-Cited2<tm2Bh a>/H	Cited2<tm2Bha>	10	Cre-mediated recombination throughout the entire epiblast of early embryos recapitulates the complete loss of function phenotype of Cited2, which include cardiac malformations, adrenal agenesis, fusion of cranial ganglia, abnormal cardiac neural crest migration, excencephaly and left right patterning defects.	Order From EMMA
TgN(UbiCFL)Ox(Cleo)				Order
CMV Gal4			None.	Order
STOCK Tg(Col2a1-cre) 1Bhr/H	Tg(Col2a1-cre)1Bhr	UN	No overt phenotype.	Order From EMMA
C3H101H-Col4a1<Bru>/ H	Col4a1<Bru>	8	(eyes - cataract - size, skin - colour) bruised.	Order From EMMA
STOCK Col4a1<Raw>/H	Col4a1<Raw>	8	Retinal ateriolar wiring. Shiny retinal blood vessels.	Order From EMMA
STOCK Col4a1<Svc>/H	Col4a1<Svc>	8	Small with vacuolar cataract. Also other eye abnormalities. Mutants are small and bruised at birth and tend to remain small throughout life. Variable eye findings, the most consistent of which is a vacuolar cataract. Other eye findings include enlarged eyes, corneal opacity, iris-corneal adhesions, iris-lens adhesions, retinal vascular abnormalities.	Order From EMMA
CON	Kitl<Sl-con>	10	(coat - colour) steel. Darkly pigmented genitalia and slightly lighter coat in heterozygote. Homozygotes are grey with dark genitalia.	Order
CON	Edar<dl>	10		Order
Connexin26-Knockout (C3H)	Gjb2	14	Heterozygotes appear wildtype and can hear, homozygous embryonic lethal.	Order
C3H;C-Gjb2<E119stop> /H	Gjb2<E119stop>	14	Homozygous lethal, heterozygotes appear as wildtypes.	Order
Connexin26<Har1> Wil d type			Homozygous lethal, heterozygotes appear as wildtypes.	Order
TgN(UbiCFL)Ox(Conrad )				Order
Cookson Mouse	Eng	2		Order
Cordon Bleu	Cobl	11	None.	Order
STOCK Scrib<Crc>/H	Scrib<Crc>	15	Neural tube defects.	Order
C3H.Cg-Scrib<Crc>/H	Scrib<Crc>	15		Order
C3H101H-Crm/H	Crm	X	(coat - colour) cream.	Order
Cry1<tm1Jhjh>	Cry1<tm1Jhjh>	10		Order
129-Ctsg<tm1.1Roes>/ H	Ctsg<tm1.1Roes>	14	Mice deficient in Ctsg are susceptible to fungal infections, despite normal neutrophil development and recruitment.	Order From EMMA
CVBA 3'/Utrophin+/-/ mdx			CVBA 3'/Utrophin+/-/mdx mice are transgenic for the dystrophin cDNA with a deletion of exons 17-48 under the control of the MCK promoter.	Order From EMMA
C3H;C-Gjb2<I128V>/H	Gjb2<I128V>	14	Heterozygotes appear wildtype and show normal hearing.	Order From EMMA
C3H;C-Chd7<Cycn>/H	Chd7<Cycn>	4	Headbobbing/circling. Heterozygotes exhibit headweaving and circling behaviour. Homozygous foetuses exhibit midgestational lethality potentially due to vascular and/or anterior neural tube defects.	Order From EMMA
D1ApA63(Knockin)				Order
C3H;C-Dfp2/H	Dfp2	4	Heterozygotes have dark pigmentation on footpads and additional areas such as tail, ears etc.	Order From EMMA
DBA/2			Non-agouti brown, pink eyes. Susceptible to audiogenic seizures. Spontaneous calcified heart lesions progress with age.	Order
C3H101H-Dbf/H	Dbf	1	Many extra toes on all feet. Homozygote lethal. Dominant, digits - number, limbs - bones, size - small, reduced viability, skull, sterility, cerebrospinal fluid??	Order From EMMA
C3H101H-Dct<slt>/H	Dct<slt>	14	Slatey.	Order
DDK				Order
C3H101H-Del(1)55H			(size - birth - weaning) small at birth and weaning.	Order
C3H101H-Del(1)57H			(size - birth, anaemia) Small at birth and seemingly anaemic.	Order
C3H101H-Del(1)58H			(size - birth - weaning, hair - colour) small at birth and at weaning with dark coats.	Order
C3H101H-Del(1)66H			(size - birth - weaning, hair - colour) heterozygote milky abdomen at birth, small at weaning.	Order
C3H101H-Del(1)70H			(size - birth - weaning, head) small at birth and weaning sometimes with a domed head.	Order
C3H101H-Del(1)6H			(size - birth - weaning, head) small at birth and weaning, with domed head.	Order
C3H101H-Del(1)42H			(size - birth - weaning - eyes) small at birth with eyes open and small at weaning with small eyes.	Order
C3H101H-Del(1)33H			(size - birth - weaning, head) small at birth and weaning, with a slightly domed head.	Order
C3H101H-Del(1)27H/H			(size - birth weaning, hair - colour) small at birth and weaning, some have white feet. No information available about homozygotes.	Order
C3H101H-Del(10)69H			(size - birth - weaning, head) heterozygotes small at birth and weaning, with domed head.	Order
Del(10)Mgf<Sl-28H>41 H	Kitl<Sl-28H>	UN	steel.	Order
C3H101H-Del(12)75H			(size - birth weaning, hair - colour, behaviour) small at birth and small at weaning with head bobbing and dark coat.	Order
C3H101H-Del(13)52H			(size - birth - weaning, hair - colour) small at birth and weaning, sometimes with dark coats.	Order
C3H101H-Del(13)80H			Del(13)80H carriers are small, with small eyes and domed heads. Del(13)80H +/+ sa has the satin phenotype.	Order From EMMA
C3H101H-Del(13)36H				Order
Del(14)Ednrb<s-163H> 10H	Ednrb<s-163H>	UN		Order
Del(14)Ednrb<s-163H> 10H	Del(14)Ednrb<s-163H> 10H	UN		Order
Del(14)Ednrb<s-174H> 15H	Ednrb<s-174H>	UN		Order
Del(14)Ednrb<s-174H> 15H	DelEdnrb<s-174H>15H	UN		Order
Del(14)Ednrb<s-175H> 14H	Ednrb<s-175H>	UN		Order
	DelEdnrb<s-175H>14H	UN
	Del(14)Ednrb<s-175H> 14H	UN
Del(14)Ednrb<s-179H> 23H	DelEdnrb<s-179H>23H	UN		Order
Del(14)Ednrb<s-179H> 23H	Ednrb<s-179H>	UN		Order
Del(14)Ednrb<s-180H> 28H	DelEdnrb<s-180H>28H	UN	Small at birth and weaning.	Order
Del(14)Ednrb<s-180H> 28H	Ednrb<s-180H>	UN	Small at birth and weaning.	Order
Del(14)Ednrb<s-181H> 31H	DelEdnrb<s-181H>31H	UN		Order
Del(14)Ednrb<s-181H> 31H	Ednrb<s-181H>	UN		Order
Del(14)Ednrb<s-182H> 32H	Ednrb<s-182H>	UN		Order
Del(14)Ednrb<s-182H> 32H	DelEdnrb<s-182H>32H	UN		Order
Del(14)Ednrb<s-184H> 29H	Dct<slt>	UN		Order
	DelEdnrb<s-184H>29H	UN
	Ednrb<s-184H>	UN
Del(14)Ednrb<s-187H> 39H	DelEdnrb<s-187H>39H	UN	(size) small with high expression.	Order
Del(14)Ednrb<s-187H> 39H	Ednrb<s-187H>	UN	(size) small with high expression.	Order
Del(14)Ednrb<s-198H> 60H	DelEdnrb<s-198H>60H	UN		Order
Del(14)Ednrb<s-198H> 60H	Ednrb<s-198H>	UN		Order
C3H101H-Del(16)51H			(size - birth - weaning, hair - colour) small at birth and weaning, some white feet.	Order
C3H101H-Del(18)20H			(size - weaining, hair - colour, tail, cleft palate) small at weaning, sometimes white feet, variable tail abnormalities, tail kinks to tight curling of tail, some cleft palates/lips seen in heterozygotes also exencephaly.	Order
C3H101H-Del(2)59H			(size - birth - weaning, genetalia - colour, head) small at birth and small at weaning with small eyes and domed/short heads and some have dark genitalia.	Order
Del(2)Sey<2H>82H	Pax6<Sey-2H>	2	Small at birth and weaning. Small or closed eyes, white feet.	Order
C3H101H-Del(2)Sey<4H >83H/H	Pax6<Sey-4H>	UN	Small eyes and sometimes small at birth.	Order
C3H101H-Del(2)Sey<4H >83H/H	Del(2)Sey<4H>83H	UN	Small eyes and sometimes small at birth.	Order
C3H101H-Del(2)35H			(size - birth - weaning, hair - colour) small at birth and weaning, sometimes white feet, occasional belly spot.	Order
STOCK Del(3)48H			Small.	Order
C3H101H-Del(3)64H			(size - birth - weaning, head) small at birth and weaning, unusual shaped heads.	Order
C3H101H-Del(4)17H			(size - birth - weaning, behaviour - waltzing, skin - colour) small at birth and weaning, waltzer type behaviour, variable white feet.	Order
C3H101H-Del(5)68H			(size - birth weaning, behaviour) small at birth and weaning with erratic behaviour.	Order
Del(5)Kit<W-34H>43H	Kit<W-34H>	UN		Order
Del(5)Kit<W-34H>43H	DelKit<W-34H>43H	UN		Order
Del(5)Kit<W-35H>47H	DelKit<W-35H>47H	UN		Order
Del(5)Kit<W-35H>47H	Kit<W-35H>	UN		Order
Del(5)Ph<2H>25H	Ph<2H>	UN	patch.	Order
C3H101H-Del(6)26H			(size - birth weaning, hair - colour) small at birth and weaning with dark (umbrous) coat.	Order
C3H101H-Del(7)49H			(size - birth - weaning, hair - colour) small at birth and weaning, dark coats, white toes. Phenotype and deletion may not be associated.	Order
C3H101H-Del(7)56H			(size - birth - weaning, hair - colour) small at weaning, some have milky abdomens.	Order
C3H101H-Del(8)50H			(size - birth - weaning, hair - colour) small at birth and weaning, with dark coats.	Order
C3H101H-Del(8)62H			(size, head, behaviour - circling) small, some with short heads, circling.	Order
C3H101H-Del(8)72H			(size - birth weaning, hair - colour, behaviour) small at birth and weaning, also dark coats. Some show circling behaviour.	Order
C3H101H-Del(8)7H			(abdomen, feet) chylous ascites.	Order
C3H101H-Del(8)74H			(feet, tail) milky abdomen, puffy feet and thick tail.	Order
C3H101H-Del(9)4H			(size - small, white spotting) low grade white head/feet tail spotting, carriers small from birth.	Order
129P2/OlaHsd-Tpcn2<G t(YHD437)Byg>/H	Tpcn2<Gt(YHD437)Byg>	7		Order
C57BL/6J-H19<tm2Wrk>	H19<tm2Wrk>	7	Deletion of the H19 transcription start site shows no effect on imprinting expression or DNA methylation.	Order From EMMA
C3H101H-Dh/H	Dh	1	dominant hemimelia, Classified at birth by absence of spleen. Toes not always abnormal. Het.show preaxial polydactyly or oligodactyly of the hind limbs, tibial hemimelia, & sometimes reduction of the femur & pubic element of the pelvic girdle, no. etc...	Order
C3H;C-Dilp3/H	Dilp3	UN	Dilated pupils.	Order From EMMA
C3H;C-Dilp4/H	Dilp4	UN	Mice carrying this mutation have permanently dilated pupils.	Order From EMMA
C3H101H-Dkf/H			(feet - colour, tail - colour, size - weaning) Darkfoot, dominant, homozygous lethal. Heterozygotes have dark foot-pads and tails, also slightly small at weaning.	Order
Dl<Slk2H>	Edar<Dl-Slk2H>	UN	Greasy coat, hairy tail.	Order
C3H101H-Edar<Dl-slk> /H	Edar<Dl-slk>	10	(hair, teeth) sleek.	Order
STOCK Tmc1<dn>	Tmc1<dn>	19	Deafness.	Order From EMMA
C3H101H-Dp(1)6H			Small at birth and weaning.	Order
C3H101H-Dp(12)7H			joined toes on hind feet.	Order
C3H101H-Dp(12)9H			dark coat and skin seen on ears, feet and tail with occasional domed head.	Order
C3H101H-Dp(13)17H			Small at birth and weaning.	Order
C3H101H-Dp(14)18H			small at birth and weaning, some have dark coats.	Order
C3H101H-Dp(14)2H			dark coat, small, white toes/feet.	Order
C3H101H-Dp(15)5H			Slightly small at weaning, some show erratic waltzing type behaviour, variable white feet/tail, dark coats.	Order
C3H101H-Dp(16)15H			Small at birth and weaning, sticky eyes, domed head.	Order
C3H101H-Dp(16)8H				Order
C3H101H-Dp(18)4H			Small with dark coats.	Order
C3H101H-Dp(2)11H			(size - birth - weaning, hair - colour, behaviour) small at birth and small at weaning with dark coat and showing abnormal behavior. i.e. shaking, head bobbing and very active.	Order
C3H101H-Dp(3)10H			(size, head) heterozygotes are usually small with a domed head.	Order
C3H101H-Dp(4)20H			Small at weaning with a short domed head. Homozygous lethality. some dark coat and low grade white spotting on the feet only was seen.	Order
C3H101H-Dp(7)1H			Small at weaning, dark coats (some).	Order
C3H101H-Dp(7)16H			small at birth and small at weaning with dark coats.	Order
C3H101H-Dp(7)19H			Small at birth and weaning.	Order
C3H101H-Dp(9)12H			Small with dark coat.	Order
C3H101H-Dp(9)14H			Small at birth and weaning, some have dark coats, short heads and twisted jaws.	Order
C3H101H-Dp(9)3H			Heterozygotes small at birth and weaning, some fused toes, pointed faces.	Order
STOCK Lmx1a<dr-J>	Lmx1a<dr-J>	1	Deafness, circling behaviour and hyperactivity in homozygotes. They have neuronal migration disorders in the cerebral cortex, cerebellum and hippocampus. White belly spots, short tails and abnormalities of the fallopian tubes (dr<2J> only)are seen in some.	Order
C3H101H-Mc1r<E-tob>/ H	Mc1r<E-tob>	8		Order
ecd			Cartilage type defect.	Order
Ednrb<s-136H>	Ednrb<s-136H>	UN	Less spotting than Ednrb<s>.	Order
C3H101H-Ednrb<s-162H >/H	Ednrb<162H>	UN		Order
C57BL-Eh/H	Eh	15	Hairy ears (Eh). Reduced pinna with tufts of hair on inner surface. Homozygous lethal. Breeding poor when crossed to C57BL/6J.	Order
ELK6K<-/->(lambda)<- /->			Production of rat kappa light chains on mouse lambda and kappa light chain knockout background.(or on mouse kappa-type light chain knockout only, with mouse lambda-type light chain being wild type instead of knockout.	Order
B6;129P2-Eltd<tm1Dge n>/H	Eltd1	3	None.	Order From EMMA
Epc1<tm1aWtsi>	Epc1	18	None.	Order From EMMA
C3H101H-Es3<c-nH>	Es3<c-nH>	11		Order
	Es3<c>	UN
	Es3<b>	UN
B6;129P2-Esr2<tm1Dge n>/H	Esr2	12	No visible phenotype.	Order From EMMA
129S9/SvEvH-Evta/H	Evta	UN	White coat with non-agouti specking and occasional non-agouti patches.	Order From EMMA
B6NDen;B6N-Slc38a10< tm2a(EUCOMM)Wtsi>/H	Slc38a10<tm2a(EUCOMM )Wtsi>	11		Order From EMMA
TgN(FLU)Ox(Fergie)				Order
C3H;C-Fer/H	Fers	4	Heterozygotes have abnormal hind limbs, vigourous touch escape and circling.	Order From EMMA
TgN(FLU)Ox(Fiona)				Order
FMLC-TM/12			Statistically elevated levels of leptin & adiponectin after overnight fasted bleeds at 12wks of age with increased bodyweight. Bodyweight & adiponectin levels still elevated after an overnight fasted bleed at 16wks of age. After DEXA analysis: statistically increased bodyweight, fat mass & % body fat.	Order
C3H101H-Fnld/H	Fnld	X	Faint lined.	Order
C3H;C-Gsdma3<Fgn>/H	Gsdma3<Fgn>	11	Mice carrying this mutation show progressive hair loss. Weanlings show a typical ragged coat phenotype. Following this mice go through several cycles of hair loss and regrowth. Adult mice eventually become almost hairless with a small amount of hair around the snout.	Order From EMMA
FNOS2			Circling, vestibular defects. Heterozygotes can be identified by mild head bobbing or circling behaviour. Mice with this behaviour usually show morphological changes in the inner ear.	Order From EMMA
Foxh1<tm1Jlw>	Foxh1<tm1Jlw>	15	Homozygous lethal at day 8 of gestation.	Order From EMMA
C3H-Foxq1<sa>/H	Foxq1<sa>	13	I=glossy coat when homozygous CON=glossy coat.	Order
FRAG 1			Affects male fertility, males with two or more copies are sterile.	Order
Frag X				Order
Fragal (CEMO_A1)				Order
TgN(FLU)Ox(Freddie)				Order From EMMA
FT	Vps33a<bf>	5		Order
	Fgf5<go>	5
	Tht	5
FTO-I367F	Fto	8		Order
FTOKOB8-B6-ACTIN-FLP E				Order
C3H101H-Axin1<Fu-kb> /H	Axin1<Fu-kb>	17	Knobbly.	Order
funny feet			Small, abnormal limbs (short and stick like).	Order
FVB/N-Tg(ACTB-cre)2M rt/J	Tg(ACTB-cre)2Mrt	UN	This Cre recombinase strain is under the human beta actin gene promoter. This strain expresses Cre recombinase in all cells of the embryo by the blastocyst stage of development.	Order
G6pd<b>			Low activity of glucose 6 phosphate dehydrogenase.	Order
STOCK G6pdx<a-m1Neu>	G6pdx<a-m1Neu>	X	Low glucose-6-phosphate dehydrogenase-a activity.	Order From EMMA
B6;129P2-Galr2<tm1Dg en>/H	Galr2<tm1Dgen>	11	No visible phenotype.	Order From EMMA
B6;129P2-Galr2<tm1Dg en>/H	Galr2	11	No visible phenotype.	Order From EMMA
Gammy (JU)			Club foot in one or both hind limbs.	Order
TgN(UminiG)Ox(Gareth )				Order
C3.C-Gars<C201R>/H	Gars<C201R>	6	Mice heterozygous for this dominant mutation exhibit low limb tone, low grip strength and poor wire manoeuvrability.	Order From EMMA
TgN(UminiG)Ox(Gavin)				Order
129-Elane<tm1(cre)Ro es>/H	Elane<tm1(cre)Roes>	10	Impaired innate immunity.	Order From EMMA
129-Elane<tm1(cre)Ro es>Ctsg<tm1.1Roes>/H	Elane<tm1(cre)Roes>	10	Impaired innate immunity.	Order From EMMA
129-Elane<tm1(cre)Ro es>Ctsg<tm1.1Roes>/H	Ctsg<tm1.1Roes>	14	Impaired innate immunity.	Order From EMMA
GENA287			Heterozygotes are small at birth and maturity with striped coat.	Order
GENA 29 (Cross 3)			Kumba mouse can be belly spot, curly tail, or spina bifida.	Order
GENA381			High Alkaline phosphatase, low cholesterols, distinguishable by blood testing. Some mutants are smaller and have a darker coat colour.	Order From EMMA
GENA394			Impaired Glucose Tolerance (IGT).	Order From EMMA
GENA111			Small at birth and weaning. Waddler behaviour. Rough coat.	Order From EMMA
C3H;C-Emx2<Pdo>/H	Emx2<Pdo>	19	Mice heterozygous for this mutation carry a dominant mutation that causes syndromic hearing loss and is possibly a novel mouse model of Leopard Syndrome. Currently known defects in affected mice include conductive hearing loss due to malformation of the ossicular chain and sensineural deafness due to an extra inner and outer row of stereocillia hair cellls in the cochlea. Heart defects are also suspected but have not been confirmed.	Order From EMMA
GENA187			High locomotive activity and arousal activity in heterozygotes.	Order From EMMA
GENA221			Heterozygotes are smaller than wildtypes.	Order From EMMA
C3H;C-Tuba1a<Jna>/H	Tuba1a<Jna>	15	Behavioural.High LMA. Heterozygotes are detected by measuring beam-splitting activity in LMA cages. Homozygosity has not been tested. GENA227 exhibits spontaneous hyperactivity in the absence of deafness and circling.	Order From EMMA
GENA316			GENA316/+ animals have poor rota rod performance.	Order From EMMA
GENA323			Large body size (+125%) and flaccid abdonimal tone.	Order From EMMA
GENA339			Mice heterozygous for this mutation have cranofacial abnormalities observed as a broad head.	Order From EMMA
GENA344			High pelvic elevation.	Order From EMMA
GENA353			No response to touch escape.	Order From EMMA
GENA357			Intermittent fits.	Order From EMMA
GENA360			Low total choloesterol and HDL cholesterol.	Order From EMMA
GENA370	Pmp22	11	Fits and marked resting tremors. Mice heterozygous for this mutation exhibit hypomyelination abnormalities and have a marked resting tremor.	Order From EMMA
GENA371			No tail.	Order
GENA377			Heterozygote animals fall off the rota rod.	Order From EMMA
GENA396			Mice heterozygous for this mutation have high blood glucose concentrations (hyperglycaemia).	Order From EMMA
GENA397			Hypoglycaemic.	Order From EMMA
C3H.C-Scn8a<Clth>/H	Scn8a<Clth>	15	Cloth-ears mice show reduced acoustic startle response and mild hearing loss from about 30 days old. Tests indicate that the peripheral neural auditory pathway is impaired in these mutants, but that cochlear function is normal. Both homozygotes and heterozygotes display paroxysmal tremor episodes with behavioural arrest. Homozygotes demonstrate a milder continuous tremor during movement and rest.	Order From EMMA
GENA401			Late onset deafness.	Order From EMMA
GENA100			Mice carrying this mutation have dark pigmentation on their footpads and additional areas such as the ears and tail. Some litter mates may also be small.	Order From EMMA
GENA115			Small at birth and weaning. Small testis.	Order From EMMA
GENA119			circling.	Order
B6J.Cg-Bfc/H			Short domed head.	Order
C3H.Cg-Bfc/H	Bfc	9	Short broad head, dark pigmentation, abnormal gait and plevic elevation. Mice heterozygous for this mutation have abnormal facial pigmentation, cranofacial abnormalities observed as broad head and skeletal abnormalities observed as an abnormal gait and elevated pelvis.	Order From EMMA
C.Cg-Bfc/H	Bfc	9	Short broad head, dark pigmentation, abnormal gait and plevic elevation. Mice heterozygous for this mutation have abnormal facial pigmentation, cranofacial abnormalities observed as broad head and skeletal abnormalities observed as an abnormal gait and elevated pelvis.	Order
GENA127			Heterozygotes have a pigmentation defect where the coat is lighter than agouti.	Order From EMMA
GENA135			Mice carrying this mutation have an abnormal gait (hunched, jerky, darting), tail rattle, evidence of aggression in arena, vigourous touch escape response and tachycardia.	Order From EMMA
GENA140			Small with short head.	Order
GENA143			Abnormal gait and waddling movement.	Order From EMMA
GENA144			Passive.	Order
GENA15			Small, extra digit.	Order
GENA151			High activity.	Order
GENA155			Heterozygotes are small with elevated pelvic limbs.	Order From EMMA
GENA160			Head shaking , belly spot, white toes.	Order From EMMA
GENA172			GENA172/+ animals have white feet and a belly spot.	Order From EMMA
GENA185			Dominant behavoiural mutant with high gait, balance problems and strong grip.	Order
C3H;C-Icst/H	Icst	2	Abnormal gait and iris corneal strands.	Order From EMMA
GENA200			Heterozygotes have a reduced or absent toe pinch response and/or reduced grip strength in SHIRPA assessment.	Order From EMMA
GENA203/mod			GENA203 mod/+ have an extra digit on one hind limb. GENA203 mod/Spgl have extra digits on all four limbs. Both have bone abnormalities.	Order
GENA214			Very active, circling, limb grasp, no toe pinch.	Order
GENA217			Low ppi.	Order
GENA228			Behaviour. Headweaving and Circling in heterozygotes.	Order From EMMA
GENA243			Low Total and HDL cholesterol.	Order From EMMA
GENA250			Low plasma alkaline phosphatase.	Order From EMMA
GENA26			Low muscle tone, belly spot, white feet, short crinkly tail.	Order From EMMA
C3H.Cg-Zic2<Ku>/H	Zic2<Ku>	14	The Kumba mouse (also known as GENA29) has three possible phenotypes, belly spot, curly tail, or spina bifida. Arose because of looped tail and or ventral spotting. Rare (~2%) instances of spina bifida were also observed. Mutation maintained by backcrosses to C3H. The C3H background seems to decrease the penetrance of the visible heterozygous phenotypes. The homozygous mutation causes mid gestation lethality, with embryos exhibiting neural tube and other defects.	Order From EMMA
GENA31			Heterozygote females have a stripey coat at 8 days indicative of X-inactivation. Hemizygous males do not survive. Phenotype of heterozygous females has not been characterised in detail.	Order From EMMA
GENA313			Poor righting reflex and small.	Order From EMMA
GENA318			Irritable at shirpa, kinky tail, high locomotive activity.	Order From EMMA
GENA321			High Startle. Heterozygotes are detected by measuring response to 110 db tones. They are hyper responsive to sudden pulses of sound. The underlying cause may be neurological or behavioural. Homozygosity has not been tested to date.	Order From EMMA
GENA327			High triglycerides.	Order
C3H;C-Alpl<Hpp>/H	Alpl<Hpp>	4	Mice with this mutation have low plasma alkaline phosphatase.	Order From EMMA
GENA342			Headweaving/headbobbing and circling in heterozygotes.	Order
C3H;C-Gck<Gena348>/H	Gck<Gena348>	11	Mice heterozygous for this mutation have high blood glucose and increased body weight.	Order From EMMA
GENA350			Abnormal gait, vigorous touch escape.	Order From EMMA
GENA359			GENA359/+ animals have a lower left eye, blunt nose, craniofacial defect.	Order From EMMA
C3H;C-Flna<Dilp2>/H	Flna<Dilp2>	X	Dilated pupils in heterozygotes.	Order From EMMA
GENA382			Animals from this stock have abnormally high levels of alanine transferase (ALT) and asparate tansferase (AST).	Order
GENA383			Inherited abnormal high levels of plasma sodium and chloride.	Order From EMMA
GENA391			Lipid and glucose perturbations.	Order From EMMA
GENA40			Dark coat.	Order From EMMA
C3H;C-Rasgrf1<enu1H> /H	Rasgrf1<enu1H>	9	Small mice when inherited through an affected male-imprinting mutation.	Order From EMMA
GENA91			Tremor.	Order From EMMA
C3H.Cg-Sho2/H			GENA93 animals have cranofacial abnormalities observed as shorthead.	Order From EMMA
TgN(UminiG)Ox(George )				Order
TgN(UminiG)Ox(Gerald )				Order
C3H/HeH-Gja8<No2>/H	Gja8<No2>	3	Cataract in lens nucleus, more severe in homozygotes.	Order From EMMA
C3H101H-Gli3<Xt>/H	Gli3<Xt>	13	Extra toes.	Order
C3H101H-Gli3<Xt-2H>	Gli3<Xt-2H>	13	Extra toes.	Order
129S2.Cg-Gnas<tm2Kel >/H	Gnas<tm2Kel>	2	There is a behavioural phenotype: response to novel environments as measured through activity in various tasks. This targeted allele has been shown to represent a null for Nesp55 protein.	Order From EMMA
B6.Cg-Gnas<tm2Kel>/H	Gnas<tm2Kel>	2	There is a behavioural phenotype, response to novel environments as measured through activity in various tasks.	Order From EMMA
TgN(UminiG)Ox(Gordon )				Order
C3H101H-Gpi1<c>/H	Gpi1<c>	7		Order
C3H101H-Gpi1<a-m1H>	Gpi1<a-m1H>	7		Order
Gpi1-s<TEM>	Gpi1<b>	UN		Order
	Gpi1<a>	UN
	Gpi1<TEM>	UN
B6;129P2-Gpr56<tm1Dg en>/H	Gpr56	8	None	Order From EMMA
129-Gca<tm1Roes>/H	Gca<tm1Roes>	2	Minimal.	Order From EMMA
TgN(UminiG)Ox(Grant)				Order
B6NDen;B6N-Snip1<tm1 a(EUCOMM)Wtsi>/H	Snip1<tm1a(EUCOMM)Wt si>	4		Order From EMMA
B6;129P2-Grm1<tm1Dge n>/H	Grm1	10	No visible phenotype.	Order From EMMA
B6;129P2-Grm4<tm1Dge n>/H	Grm4	17	No visible phenotype.	Order From EMMA
B6;129P2-Grm5<tm1Dge n>/H	Grm5	7	No visible phenotype	Order From EMMA
B6;129P2-Grm8<tm1Dge n>/H	Grm8	6	No visible phenotype	Order From EMMA
C3H101H-Gs/H	Gs	X	Greasy.	Order
GtRosa26LacZ<tm1Col>			No obvious phenotype.	Order From EMMA
B6J;C-Guth/H			Huntington’s disease, enhancer of tremor onset.	Order
Hba<c2>	Hba<c2>	UN		Order
Hba<c2>	Hba<f>	UN		Order
Hba<cm>	Hba<cm>	UN		Order
Hba<cm>	Hba<f>	UN		Order
Hbb<d3>	Hbb<d3>	UN		Order
C3H101H-Hbb<d4>/H	Hbb<d4>	7		Order
C3H101H-Hbb<d5>/H	Hbb<d5>	UN		Order
Hbb<d6>	Hbb<d6>	UN		Order
C3H101H-Hbb<d7>/H	Hbb<d7>	UN		Order
B6N-Hbp1<not yet ass igned>/H	Hbp1	12		Order From EMMA
B6N;B6N-Herc3<tm1a(E UCOMM)Wtsi>/WtsiH	Herc3<tm1a(EUCOMM)Wt si>	6	None.	Order From EMMA
C57BL/6J-Nox3<het>/H	Nox3<het>	17	Heterozygotes can have abnormal circling behaviour & hyperactivity. Homozygotes also exhibit a subtle head tilt.	Order
Hira<neo>			Early embryonic lethality	Order
Histidinaemic			Grey	Order
129-Foxa2<tm1Jrt>/H	Foxa2<tm1Jrt>	2	Homozygous lethal at day 8 of gestation.	Order From EMMA
HNF4 cre	Hnf4a	2	Homozygous lethal at mid gestation due to defects in liver formation.	Order From EMMA
Hox11 KO/unr5			Hox11 KO produces spleenless mice. uNR5 causes truncation (deletion of C1 and C2) of IgM H-chain.	Order
Hoxa3<tm1(cre)Moon>	Hoxa3<tm1(cre)Moon>	6		Order
C3H101H-Gnrh1<hpg>/H	Gnrh1<hpg>	14		Order
Hprt				Order
C3H101H-Aifm1<Hq>/H	Aifm1<Hq>	X		Order
C3H101H-Hr<hr>Ednrb< s>/H	Hr<hr>	14	Hairless.	Order
HSA-Mini George				Order
HSA-mini Grant				Order
STOCK hsh/H	hsh	3	hind shaker	Order
HSP27 WT High Copy L ine			No phenotype in transgenic carriers.	Order From EMMA
HSP27 WT Low Copy Li ne			No phenotype in transgenic carriers.	Order From EMMA
HSP27 WT PrP Promote r Line			No phenotype in transgenic carriers	Order From EMMA
HT	Gdf5<bp>	2		Order
	Pldn<pa>	2
	Mlph<ln>	1
	Ap3b1<pe-H>	UN
C3H101H-Hum/H			Heterozygotes have very dark stripe down the back, homozygotes very dark all over.	Order
B6NDen;B6N-Tnfaip1<t m1a(EUCOMM)Wtsi>/H	Tnfaip1<tm1a(EUCOMM) Wtsi>	11		Order From EMMA
C3h101H-Hw/H			Small at birth and weaning, waltzing and circling phenotype. Homozygotes probably die before birth.	Order
Igfn1_KD1				Order
IGT/10			Double heterozygous mice have type II diabetes.	Order
B6;129P2-Il8ra<tm1Dg en>/H	Cxcr1<tm1Dgen>	1	No visible phenotype.	Order From EMMA
IM	Prnp	2	Dilute brown coat.	Order
C3H101H-In(1)5H			White toes and spotting. Animals tend to be small	Order
STOCK In(2)2H	A<w>	2	Phenotypic effect on agouti locus.	Order
STOCK In(2)2H	As	2	Phenotypic effect on agouti locus.	Order
STOCK In(2)5Rk	Pldn<pa>	2	black with a tan belly	Order
	Pax1<un>	2
	a<t>	2
C3H101H-In(5)9Rk			reduced fertility in both sexes	Order
STOCK In(X)IH				Order
STOCK In(X)3H	Eda<Ta>	X		Order
STOCK In(X)3H	Atp7a<Mo-blo>	X		Order
In(YLS)Lub(Y<m>)				Order
B6NDen;B6N-Cyb561<tm 1a(EUCOMM)Wtsi>/H	Cyb561<tm1a(EUCOMM)W tsi>	11		Order From EMMA
INH/17			Trembler mutation with high stepping gait.	Order From EMMA
INH/18			Trembler mutation with high stepping gait.	Order From EMMA
INH/6			Heterozygous females are striped. Hemizygous males have no guard hairs, hair on tails, normal teeth, very little hair behind the ears. Homozygous females look like hemizygous males.	Order From EMMA
INH/8			Trembler mutation (poor inheritance).	Order From EMMA
Invs<inv>	Invs<inv>	4	Homozygous embryos develop situs inversus.	Order From EMMA
Icst	Icst	2	Abnormal gait, iris-corneal strands. Heterozygotes have variable eye phenotypes - corneal opacity/bulging, iris-corneal adhesion, irregular pupil, cataracts, some appear to have secondary glaucoma. May have poor penetrance.	Order
C3H101H-Is(1;13)4H/H			Small at birth and weaning.	Order
STOCK Is(7;1)40H			males are sterile.	Order
C3H101H-Is(In7;X)1Ct /H				Order
C3H101H-Is(In7;X)1Ct -Xce<a>/H	Xic<a>	X	Non-random X-inactivation	Order
C3H101H-Is(In7;X)1Ct -Xce<b>/H	Xic<b>	X		Order
Isl1<tm1(cre)Cos>	Isl1<tm1(cre)Cos>	13		Order
Isl1<tm1(cre)Sev>	Isl1<tm1(cre)Sev>	13		Order
STOCK a<18H>/H	a<18H>	2	Homozygotes are non-agouti with very dark pinna hairs. A/a<18H> looks wild-type. a/a<18H> look umbrous i.e. non-agouti with agouti hairs along side of body and on the belly.	Order
STOCK Dnahc11<iv>/H	Dnahc11<iv>	12	Situs inversus viscerum.	Order From EMMA
jas1			Wavy coat and curly whiskers.	Order
C3H.Cg-Fbxo11<Jf>/H	Fbxo11<Jf>	17	Deaf.	Order From EMMA
129P2/OlaHsd-Map3k1< Gt(YTC001)Byg>/H	Map3k1	13	Full description available from Europhenome	Order
C3H101H-Plp1<jp>/H	Plp1<jp>	X		Order
JPX	Glo1<b>	UN		Order
	Ldh2<b>	UN
	Hk1<b>	UN
	Sdh1<b>	UN
B6.A-Ush1g<js>/J	Ush1g<js>	11	Deafness.	Order
JU/FaCt-+<a> +<c>				Order
Ju/FaCt-+<c>				Order
C3H.Cg-Mecom<Jbo>/H	Mecom<Jbo>	3	Late onset deafness, extra digit, reduced body weight, craniofacial defect.	Order From EMMA
K10T+/-	Krt10<tm1Tmm>	11	K10T mice show a phenotype in the epidermis and in tongue, esophagus and forestomach. Homozygous pups die on the first day after birth from dehydration due to generalised blistering within the epidermis. Heterozygous mice look normal at birth and develop a progressive thickening of the skin and hyperkeratosis. Their skin is scaly. Heterozygotes breed normally.	Order From EMMA
B6;129P2-Kcnj15<tm1D gen>/H	Kcnj15	16	Kir4.2 potassium channel knockout. Phenotype as yet undetermined	Order From EMMA
Khk-a<tm1.1Ls>				Order
Khk-N<tm1(neo)Ls>				Order
C3H101H-Kit<W-19H>	Kit<W-19H>	5	dominant spotting	Order
CBA/H-Kit<W-27H>/H	Kit<W-27H>	5	Dominant spotting.	Order
C3H-Kit<W-28H>	Kit<W-28H>	5	dominant spotting	Order
C3H-Kit<W-29H>	Kit<W-29H>	5	dominant spotting	Order
Kit<W-30H>	Kit<W-30H>	UN	dominant spotting	Order
C3H101H-Kit<W-31H>/H	Kit<W-31H>	UN	Dominant spotting.	Order
Kit<W-32H>	Kit<W-32H>	UN	Dominant spotting.	Order
Kit<W-33H>	Kit<W-33H>	UN	dominant spotting	Order
C3H101H-Kit<W-36H>	Kit<W-36H>	5	Dominant spotting.	Order
C3H101H-Kit<W-38H>/H	Kit<W-38H>	UN	dominant spotting	Order
C3H101H-Kit<W-bd>/H	Kit<W-bd>	5	White band in trunk region.	Order From EMMA
C3H101H-Kit<W-ct>/H	Kit<W-ct>	5	Cattanach's dominant spotting	Order
C3H.Cg-Kit<W-e>/H	Kit<W-e>	5	Heterozygotes have coat spots. Homozygosity is lethal.	Order From EMMA
C3H101H-Kit<W-sh>/H	Kit<W-sh>	5	Sash	Order
Kit<W-sh>l	Kit<W-shl> ??	UN		Order
C57BL-Kit<W-v>/H	Kit<W-v>	5	Viable dominant spotting	Order
C3H;C-Kit<W-39H>	Kit<W-39H>	5	Heterozygotes have a white belly spot and occasionally a white head blaze. Homozygotes have not been identified and they may die in utero	Order
C3H-Koa/H	Koa	15	Heterozygotes have hairy ears and muzzle, homzygotes are slightly more extreme.	Order
B6NDen;B6N-Fam117b<t m1a(EUCOMM)Wtsi>/H	Fam117b<tm1a(EUCOMM) Wtsi>	1		Order From EMMA
C3H101H-Sox<lcc>/H	Sox2<lcc>	3	light coat circler	Order
C3H101H-Lct/H			Light coat.	Order
C3H;C-Lcl/H	Lcl	UN	Lens cloudy. Cataracts. Mice heterozygous for this mutation show progressive cataract formation, with total opacity at approximately 3 months. Mice homozygous for this mutation have small eyes and total lens opacity at 4-5 weeks.	Order From EMMA
STOCK Rb(6.15)1Ald-M ip<Cat-Lop>/H	Mip<Cat-Lop>	10	Lens opacity.	Order
C3H;C-Pax6<Leca1>/H	Pax6<Leca1>	2	Heterozygotes have a central indentation and may have small eyes, irregular pupils and lens corneal adhesions	Order From EMMA
C3H;C-Pax6<Leca2>/H	Pax6<Leca2>	2	Heterozygotes have small eyes, corneal opacities and cataracts.	Order From EMMA
C3H;C-Pax6<Leca3>/H	Pax6<Leca3>	2	Mutants may have central corneal opacity, small eyes, dilated pupils and lens-corneal adhesion.	Order From EMMA
Lepr<db>	Lepr<db>	4	Recessive misty mutation is present. Homozygotes become obese at 3-4 weeks of age. Elevation of plasma insulin begins at 10-14 days and of blood sugar at 4-8 weeks. Homozygotes die by 10 months of age.	Order
C3H101H-Li/H	Li	X	Lined.	Order
LII	Mcoln3<Va>	3		Order
	Gli3<Xt>	13
	T	17
LIII	Cdh23<v>	10		Order
	Mlph<ln>	1
	Hps1<ep>	19
	Sgk3<fz>	1
Lim-1 (Lhx-1)	Lhx1<tm1Bhr>	11	Homozygous lethal at day 10 of gestation.	Order From EMMA
Line # 46 - Fused lo be				Order
Line # 48b - Unbranc hed			Fusion of cranal and medial lung lobes; kidneys are small, lack medulla; lacrimal glands have less epithelium branching	Order
LIVA	Tyrp1<b>	4		Order
	Tgfa<wa1>	6
	Tyr<c-ch>	7
	Myo5a<d>	9
	Bmp5<se>	9
	Ednrb<s>	14
	a	2
LL	Gdf5<bp-H>	UN	limb - short legs and digits affected.	Order
	Pldn<pa>	UN
	Mlph<ln>	UN
LMWP3			Low Molecular Weight Protein (LMWP) in the urine which is an indicator of proximal tubule dysfunction in the kidney.	Order
Lnk -/-				Order
Lo Moe			None.	Order From EMMA
C3H101H-Dync1h1<Loa> /H	Dync1h1<Loa>	12	Legs at odd angle.	Order From EMMA
C.Cg-Lpk/H	Lpk	UN	Short-limbed phenotype in both fore- and to a lesser extent hind-limbs. Mice have short limbs (achondroplasia).	Register Interest
C3H.Cg-Lpk/H	Lpk	UN	Short limbs (achondroplasia).	Order From EMMA
Loop tail	Vangl2<Lp>	1	Ltap<Lp>/+ mice exhibit a tail defect. Ltap<Lp>/Ltap<Lp> mice exhibit severe neural tube defect (die at birth).	Order
STOCK Lop4/H	Lop4	2	Lens opacity.	Order
STOCK Lop6/H	Lop6	UN	Lens opacity	Order
STOCK Lop9/H	Lop9	UN		Order
B6;129P2-Lphn2<tm1Dg en>/H	Lphn2	3	None	Order From EMMA
LR8	Hps6<ru>	19		Order
	Gdf5<bp>	2
	Bmp5<se>	9
	Hps5<ru2>	7
	Myo5a<d>	9
	a	2
	Oca2<p>	7
	Hps1<ep>	19
ls<rrw>	Edn3<ls-rrw>	UN	Homozygotes usually die before weaning but have a predominantly white coat with pigmental rump.	Order
B6NDen;B6N-Ttll4<tm1 a(EUCOMM)Wtsi>/H	Ttll4<tm1a(EUCOMM)Wt si>	1		Order From EMMA
LVC	Egfr<wa2>	11	Jerker, homozygotes exhibit jerky behaviour. Spontaneous. waved 2, homozygotes have wavy fur. Spontaneous. pe<H>, homozygotes have a light coat. Spontaneous. mahoganoid, homozygotes have a dark coat. Spontaneous.	Order
	Espn<je>	4
	Mgrn1<md>	16
	Ap3b1<pe-H>	UN
LVI	Kitl<Sl-gbH>	UN	Toes fused,(8) black coat,(8) belly spots,(10) light coat,(10) behavioural (18)	Order
LVI	Mc1r<E-so>	UN		Order
M1073B			Embryonic lethal.	Order From EMMA
M1185B			Embryonic lethal	Order From EMMA
M1239B			Embryonically lethal	Order From EMMA
M1616B			Embryonic lethal	Order From EMMA
M1645B			Embryonic lethal	Order From EMMA
M241B			Embryonically lethal	Order From EMMA
M369B			Embryonic lethal	Order From EMMA
M412B			Embryonic lethal	Order From EMMA
M54B			Embryonic lethal	Order From EMMA
M624B			Embryonic lethal	Order From EMMA
M876B			Embryonically lethal	Order From EMMA
C3H101H-ma-Mcoln3<Va >/H	ma	3	Mcoln3<Va> heterozygotes are deaf mice that have variegated coats, they also circle and/or headtoss. ma/ma mice have scruffy coats.	Order
C3H101H-ma-Mcoln3<Va >/H	Mcoln3<Va>	3		Order
C3H101H-Maf<tm1Glm>/ H	Maf<tm1Glm>	8	Homozygotes have eye defects, are small and shaky, and may die before adulthood.	Order
C3H-Maf<Ofl>/H	Maf<Ofl>	8	Heterozygotes-opaque flecks in lens; homozygotes- very small eyes, most die at birth through failure to feed, survivors small, trembly, and develop nephritis. Dominant cataract	Order
C3H101H-Maf<Ofl>/H	Maf<Ofl>	8		Order From EMMA
Mafb<Krml-kr>;we; (K reisler)	we	2		Order
Mafb<Krml-kr>;we; (K reisler)	Mafb<kr>	2		Order
129P2/OlaHsd-Mkrn1<G t(RRB087)Byg>/H	Mkrn1<Gt(RRB087)Byg>	6	No abnormal phenotype detected.	Order
TgN(DSPM36)1886OxAna t				Order
TgN(DSPM36)1892OxAna t				Order
MB				Order
MBT1			Lack of marble burying. Mutant mice fail to bury marbles in sawdust when left for a period of 30 minutes.	Order From EMMA
MBT2			Low anxiety, marble mutant	Order From EMMA
MBT3			Low anxiety, marble mutant.	Order From EMMA
MBTR2			Lack of marble burying.	Order From EMMA
MBTR3			Lack of marble burying.	Order From EMMA
MC-1			Phenotypically normal	Order
B6;129P2-Mc2r<tm1Dge n>/H	Mc2r	18	No visible phenotype.	Order From EMMA
MCA/mdx				Order From EMMA
B;CBACa-Dmd<mdx>Tg(C KMM-tTA)A3Rhvh/H	Tg(CKMM-tTA)A3Rhvh	UN	MCK-tTA/mdx mice contain the muscle specific creatine kinase (MCK) promoter driving the tetracycline regulated transactivator (tTA).	Order From EMMA
B;CBACa-Dmd<mdx>Tg(C KMM-tTA)A3Rhvh/H	Dmd<mdx>	X		Order From EMMA
Mcpt1<tm1Hrpm>			Lack of Mcpt-1 expression.	Order
C3H101H-Mgrn1<md-nc> /H	Mgrn1<md-nc>	16	nonagouti curly	Order
mdx	Dmd<mdx>	X	X-linked muscular dystrophy.	Order
STOCK Dmd<mdx-3Cv>/H	Dmd<mdx-3Cv>	X		Order
Mesp1<tm2(cre)Ysa>	Mesp1<tm2(cre)Ysa>	7		Order
C3H;C-Chd7<Mt>/H	Chd7<Mt>	4	Heterozygotes exhibit head weaving and circling behaviour. Homozygotes exhibit midgestational lethality possibly due to vascular defects seen in the anterior neural tube.	Order From EMMA
C3H101H-Kitl<Sl-10H> /H	Kitl<Sl-10H>	10	steel	Order
C3H101H-Kitl<Sl-12H> /H	Kitl<Sl-12H>	10	steel	Order
C3H101H-Kitl<Sl-13H> /H	Kitl<Sl-13H>	UN		Order
C3H101H-Kitl<Sl-14H> /H	Kitl<Sl-14H>	UN	Steel.	Order
C3H101H-Kitl<Sl-15H> /H	Kitl<Sl-15H>	UN	Steel.	Order
C3H101H-Kitl<Sl-17H> /H	Kitl<Sl-17H>	10	steel	Order
C3H101H-Kitl<Sl-18H> /H	Kitl<Sl-18H>	10	steel	Order
C3H101H-Kitl<Sl-20H> /H	Kitl<Sl-20H>	UN	Steel.	Order
C3H101H-Kitl<Sl-21H> /H	Kitl<Sl-21H>	UN		Order
C3H101H-Kitl<Sl-22H> /H	Kitl<Sl-22H>	UN	Steel.	Order
C3H101H-Kitl<Sl-23H> /H	Kitl<Sl-23H>	UN	Steel.	Order
C3H101H-Kitl<Sl-24H> /H	Kitl<Sl-24H>	UN	Steel.	Order
C3H101H-Kitl<Sl-25H> /H	Kitl<Sl-25H>	10	steel	Order
C3H101H-Kitl<Sl-26H> /H	Kitl<Sl-26H>	UN	Steel, greyish fur, pale feet and tail with occasional head dots and belly spots, anaemia.	Order
Kitl<Sl-27H>	Kitl<Sl-27H>	UN	Steel, greyish fur, pale feet and tail with occasional head dots and belly spots.	Order
C3H101H-Kitl<Sl-29H> /H	Kitl<Sl-29H>	UN	Steel, greyish fur, pale feet and tail with occasional head dots and belly spots, anaemia, no survival past a few days after birth.	Order
C3H101H-Kitl<Sl-30H> /H	Kitl<Sl-30H>	UN	Steel, greyish fur, pale feet and tail with occasional head dots and belly spots.	Order
C3H101H-Kitl<Sl-31H> /H	Kitl<Sl-31H>	UN	Steel, greyish fur, pale feet and tail with occasional head dots and belly spots, anaemia.	Order
C3H101H-Kitl<Sl-32H> /H	Kitl<Sl-32H>	UN	Steel, greyish fur, pale feet and tail with occasional head dots and belly spots, anaemia, high pre-implantation loss - homozygotes die early in development, some live foetuses were also anaemic.	Order
C3H101H-Kitl<Sl-33H> /H	Kitl<Sl-33H>	UN	Steel, greyish fur, pale feet and tail with occasional head dots and belly spots. Anaemia.	Order
Mgf<Sl-34H>, T(19;11 )75H	Kitl<Sl-34H>	UN		Order
C3H101H-Kitl<Sl-8H>/ H	Kitl<Sl-8H>	10		Order
C3H101H-Kitl<Sl-9H>/ H	Kitl<Sl-9H>	10	steel	Order
C3H101H-Kitl<Sl-pan> /H	Kitl<Sl-pan>	10	Steel-panda.	Order
C3H101H-cw-Bmp5<se>t k/H	cw	9	Kinky tail.	Order
	tk	9
	Bmp5<se>	9
GENA163	Mitf<Mi-H>	UN	Microphthalmia. Dominant mutant with small eyes, Mi-like. Heterozygotes are paler, they have head and belly spots. Homozygotes are white with no eyes.	Order
B6N;B6N-Mier1<tm1a(E UCOMM)Wtsi>/WtsiH	Mier1<tm1a(EUCOMM)Wt si>	4	None.	Order From EMMA
Mitf<Mi-wh>, px	Mitf<Mi-wh>	6	het. light coated & light ears & sometimes a belly spot. hom. Mitf<Mi-wh> white with slight micropthalmia, Forelimbs often affected with absence of digets & sometimes ulna. Large foramen in scapula. All feet have epidermal papillae etc.	Order
Mitf<Mi-wh>, px	Wnt7a<px>	6		Order
MLO			c<62chH>/c<62chH> homozygotes have a grey coat colour, c/c<62chH> trans-heterozygotes have a cream coat colour and ruby coloured eyes.	Order From EMMA
C3H101H-Minute/H	Minute	7	Minute.	Order
MOD Fused Toes			Syndactyly	Order
TgN(DSPM36)1892OxAna t				Order
C3H;C-Mtu/H	Mtu	12	Kinky tail, deaf, belly spot. Heterozygotes exhibit abnormal tail morphology, are deaf, and have belly spots that are characteristic of neural crest defects. Homozygotes, do not appear to be viable, as they have an open neural tube.	Order From EMMA
C3H101H-Mdh1<am1H>/H	Mdh1<am1H>	11		Order
TgN(DSPM36)1327OxAna t				Order
MR			Albino, rough kinked whiskers	Order
C57BL/6Apb-Zap70<mrt le>/Apb	Zap70<mrtle>	1	Identified by severe reduction in T cell numbers in blood. Zap70 protein expression of mrt/mrt thymocytes was 25% of +/+ thymocytes. Het mice, mrt/+ have normal levels of CD4+ and CD8+ thymocytes but Zap70 protein expression is two-fold lower.	Order From EMMA
B6.Cg-Mro<tm1H>/H	Mro<tm1H>	18	No visible phenotype.	Register Interest
Mta1<tm1aWtsi>	Mta1	12	None	Order From EMMA
C3.Cg-Mfl/H				Order
MUHi			Long term growth selected line.	Order
MULi			Long term growth selected mouse line.	Order
MURB125			Limbs and bones are shorter than normal	Order
MURB151			Heterozygotes have light grey coat , darker grey points on ears, nose and tail. Can be classified at 2-3 days old as the pigmentation of the skin is visibly different.	Order
CAST/EiJH				Order
SPRET/EiJH				Order
MUT1096			Small with broad, domed head.	Order
MUT1152			Homozygous post-implantation lethal. Heterozygotes are small with cranial doming, pop eyes, distal nasal bone with occasional indications of cleft.	Order
MUT1154			Small at birth and small at weaning with cranial doming, variably wide between eyes and shortened nasal passage.	Order From EMMA
MUT1264			Craniofacial and behavioural mutant with distal low degree tail kink. Homozygous pre-implantation lethal. Heterozygotes have a flat skull, short, blunt tails with a low degree distal kink and some have white feet. Behavioural abnormalities include head bobbing and erratic behaviour but they can swim. Small at birth and weaning with a high incidence of exencephaly in fetuses.	Order From EMMA
MUT1275			ear/ tail/ white spotting	Order
MUT1293			Small at birth and weaning. Broad head, bulging eyes, some have ear problems, ie. A build up of cartilage.	Order From EMMA
MUT1305			Craniofacial. Small, white feet, some domed heads, wide between eyes which may bulge.	Order From EMMA
MUT1397			Tail kinks.	Order From EMMA
MUT1425			Mutation causes typical chylous ascites-like symptoms - milky abdomen at birth and puffy feet and tail in older animals.	Order
MUT1454			Small at birth and weaning, white feet, short kinky tail. Some have odd behaviour - swaying, leaning, head bobbing	Order
MUT1477			milky abdomen at birth, small at weaning	Order
MUT1488			Small at birth and weaning. They have small eyes, very few have domed heads, some have white toes	Order From EMMA
MUT1490			Mutation causes typical chylous ascites-like symptoms - milky abdomen at birth and puffy feet and tail in older animals.	Order
MUT1544			Small at birth with bruised type appearance. Bloody areas beneath the skin, most common around the belly and abdomen - some around the neck and back legs. Small at weaning, most have a domed head	Order From EMMA
MUT1556			Small with white feet, some have belly spot. Some show head bobbing and blunt and/or kinky tails.	Order
MUT1602			Small at birth and weaning with white hind feet, short tail and head bobbing. Mice have shorter kinky tails. They have waltzing/head bobbing behaviour. Some are small in size and have white feet.	Order From EMMA
MUT1679			Mice are small at birth and weaning, they have white feet and shorter kinky tails. Some have domed heads i.e skeletal effects and some display behavioural abnormalities i.e head bobbing. Occasional nasal cleft.	Order
MUT1681			Small with white feet. Tails commonly severely shortened, kinked or curled. Some have broad, deep, short head, often with nasal stripe	Order
MUT1696			Small in size with head bobbing. Heterozygotes are small at birth and weaning with head bobbing. Size and behavioural mutation. Unlikely homozygotes survive as evidence of pre implantation loss. Best bred through the male as females behaviour makes them poor carers for their young.	Order
MUT1704			Small at birth and weaning. Domed/pointy heads, some with fused toes.The original female was small at birth and weaning with fused hind toes, slightly domed head, whitish toes and tail tip. The offspring phenotype varied, many were small, the fusing of toes only involved the soft tissue not bone. These embryos were generated by IVF with MUT/1704.3d male; small with kink in tail at birth. Small and runty at weaning with dark coat, pointy face and closed eyes.	Order
MUT1756			Offspring look normal until 6 weeks when fur becomes sparse, and thus classification prior to 6 weeks not possible in heterozygotes. Small at birth and weaning. Fate of homozygotes not yet determined.	Order
MUT921			Key feature is a short broad head, wide between eyes, shortened nasal passage with occasional indication of cleft. White feet and belly spots also seen. Small at birth and weaning. Recovery at birth low due to prenatal loss of foetuses with more extreme head abnormality.	Order From EMMA
STOCK Muted<mu>/H	Muted<mu>	13	Muted. Lighter coat.	Order
MUTN212			Circling, limb grasp & trunk curl.	Order
MUTN673			Small, deaf.	Order
MUTN777			Right eye missing, very active, circling	Order
MUTN873			Small, deep set eyes, short face, nose bends to left, upper teeth bent back, nose crooked, hunched, high gait & pelvic elevation, no abdominal tone, slow heart rate.	Order
MUTS 1/14			Small eye mutation	Order From EMMA
B6NDen;B6N-Mxra7<tm1 a(EUCOMM)Wtsi>/H	Mxra7<tm1a(EUCOMM)Wt si>	11		Order From EMMA
Myl2<tm1(cre)Krc>	Myl2<tm1(cre)Krc>	5		Order
Myo7a<sh1-9J>	Myo7a<sh1-9J>	7	Shaker.	Order
Myo5a<d-100H>	Bmp5<se-m>	UN		Order
Myo5a<d-100H>	Myo5a<d-100H>	UN		Order
Myo5a<d-50H>	Bmp5<se>	9		Order
Myo5a<d-50H>	Myo5a<d-50H>	UN		Order
Myo5a<d-51H>	Bmp5<se>	9	(fits?) opisthotonic lethal	Order
Myo5a<d-51H>	Myo5a<d-51H>	UN	(fits?) opisthotonic lethal	Order
Myo5a<d-53H>	Bmp5<se>	9	(fits?) opisthotonic lethal	Order
Myo5a<d-53H>	Myo5a<d-53H>	UN	(fits?) opisthotonic lethal	Order
Myo5a<d-82H>	Bmp5<se>	9		Order
Myo5a<d-83H>	Bmp5<se>	9	(fits?) opisthotonic lethal	Order
Myo5a<d-83H>	Myo5a<d-83H>	UN	(fits?) opisthotonic lethal	Order
Myo5a<d-84H>	Bmp5<se>	9	(fits?) opisthotonic lethal	Order
Myo5a<d-84H>	Myo5a<d-84H>	UN	(fits?) opisthotonic lethal	Order
Myo5a<d-85H>	Bmp5<se>	9	(fits) opisthotonic lethal	Order
	Myo5a<d>	9
	Myo5a<d-85H>	UN
C3H101H-Myo5a<d-86H> /H	Bmp5<se>	9	(fits?) Opisthotonic lethal.	Order
	Myo5a<d>	9
	Myo5a<d-86H>	UN
Myo5a<d-88H>	Myo5a<d>	9	(fits?) opisthotonic lethal	Order
	Bmp5<se>	9
	Myo5a<d-88H>	UN
Myo5a<d-89H>	Myo5a<d>	9		Order
	Bmp5<se>	9
	Myo5a<d-89H>	UN
Myo5a<d-90H>	Myo5a<d>	9	(fits?) opisthotonic lethal	Order
	Bmp5<se>	9
	Myo5a<d-90H>	UN
C3H101H-Myo5a<d-91H> /H	Bmp5<se>	9		Order
	Myo5a<d>	9
	Myo5a<d-91H>	UN
Myo5a<d-92H>	Bmp5<se>	9	(fits?) opisthotonic lethal.	Order
	Myo5a<d>	9
	Myo5a<d-92H>	UN
Myo5a<d-93H>	Myo5a<d>	9	(fits?) opisthotonic lethal	Order
	Bmp5<se>	9
	Myo5a<d-93H>	UN
C3H101H-Myo5a<d-97H> /H	Myo5a<d>	9		Order
	Bmp5<se>	9
	Myo5a<d-97H>	UN
Myo5a<d<105H>	Myo5a<d-105H>	UN		Order
Myo5a<d<52H>	Myo5a<d-52H>	UN		Order
C3H101H-Myo5a<d-58H> Bmp5<se>/H	Myo5a<d-58H>	UN	Homozygous lethal.	Order
Myo5a<d<61H>	Myo5a<d-61H>	UN		Order
Myo5a<d<78H>	Myo5a<d-78H>	UN		Order
Myo5a<d<80H>	Bmp5<se>	9		Order
Myo5a<d<80H>	Myo5a<d-80H>	UN		Order
CBB8-Myo7a<26SB>	Myo7a<26SB>	7	Shaker 1 allele. Homozygotes exhibit almost constant circling behaviour. Heterozygotes and wildtypes are indistinguishable from each other.Homozygotes show no preyer reflex. These Myo7a mutants do have severe hearing and vestibular abnormalities. While their retinas do not show any anatomical degeneration, there have been reports of retinal abnormalities.	Order From EMMA
CBB8-Myo7a<3336SB>	Myo7a<3336SB>	7	Shaker.	Order From EMMA
Myo7a<sh1-4494SB>	Myo7a<4494SB>	7	shaker	Order From EMMA
Myo7a<sh1-4626SB>	Myo7a<4626SB>	7	Shaker. Deafness, headshaking, circling	Order From EMMA
Myo7a<sh1-6J>	Myo7a<sh1-6J>	7	Shaker.	Order
Myo7a<sh1-8165SB>	Myo7a<sh1-8165SB>	UN	shaker. Homozygotes exhibit almost constant circling behaviour. Heterozygotes and wildtypes are indistinguishable from each other. Homozygotes show no preyer reflex. Homozygote females will not rear litters	Order
Myo7a<Sh1-816SB>	Myo7a<816SB>	7	Homozygotes exhibit almost constant circling behaviour. Heterozygotes and wild types are not distinguishable from each other. Homozygotes show no preyer reflex	Order From EMMA
Myo7a<sh1>	Myo7a<sh1>	7	shaker	Order
TgN(DSPM36)1668OxAna t				Order
C3H101H-Nan/H	Nan	8	neonatal anaemia	Order
C3H;C-Nano/H	Nano	X	Heterozygotes have small narrow faces. With aging, they develop patches of white hairs on their back. Hemizygous males are presumed to die in utero.	Order From EMMA
B6.129P2-Nat2<tm1Esi m>/H	Nat2<tm1Esim>	8	None.	Order From EMMA
B6;129-Scn10a<tm3(cr e/ERT2)Jnw>/H	Scn10a<tm3(cre/ERT2) Jnw>	9	None observed (heterozygous Nav1.8-CreERT2 can express enough Cre to delete the floxed fragement, but it does not affect the expression of Nav1.8 in Nav1.8 positive neurons in DRG).	Order From EMMA
B6;129P2-Nek6<tm1Dge n>/H	Nek6	2	No visible phenotype.	Order From EMMA
Nephertiti			No visible phenotype. Mice develop nephrotic range proteinuria at a young age and has abnormal liver histology, similar to Lafora body disease.	Order From EMMA
129S/SvEvNimrH-Nespa s<tm1Jop>/H	Nespas<tm1Jop>	2	Heterozygotes with paternal inheritance of deletion die within 1-2 days of birth. Heterozygotes with maternal inheritance of deletion appear normal.	Order
B6NDen;B6N-Nipsnap1< tm1a(EUCOMM)Wtsi>/H	Nipsnap1<tm1a(EUCOMM )Wtsi>	11		Order From EMMA
Nkx2-5<tm1(cre)Rjs>	Nkx2-5<tm1(cre)Rjs>	17		Order
Nmnat1<tm2Cole>			None	Order
C3H-Crygb<nop>/H	Crygb<nop>	1	nuclear opacity. Dominant cataract	Order
No fur			Curly whiskers and progressive hair loss.	Order From EMMA
C3H;102-Cryge<No3>/H	Cryge<No3>	1	Nuclear opacity 3. Dominant cataract.	Order From EMMA
Nodal<tm3Rob>	Nodal<tm3Rob>	10	Het shows no phenotype, homozygous results in disrupted L/R patterning.	Order
NOD			Age related onset of diabetes.	Order
NPA31-B4			Offspring inheriting the targeted construct paternally do not feed, are hypoactive and die within a few hours.	Order
C3H-Npp/H	Npp	5	nuclear-posterior polar opacity. Dominant cataract	Order
B6;129P2-Npy6r<tm1Dg en>/H	Npy6r	18	No visible phenotype.	Order From EMMA
B6;129P2-Nr1d2<tm1Dg en>/H	Nr1d2	14	No visible phenotype.	Order From EMMA
C3H;102-Casr<Nuf>/H	Casr<Nuf>	16	Small flecks in lens nucleus, difficult to see in heterozygote, clearer in homozygotes. The Nuf mice also exhibit ectopic calcification.	Order From EMMA
NVPD				Order
Och, Re<wc>	Krt27<Re-wc>	11	Och, ochre. Re<wc>, wavy coat.	Order
Och, Re<wc>	Och	4	Och, ochre. Re<wc>, wavy coat.	Order
C3H101H-Gnas<Oedsml> /H	Gnas<Oedsml>	2	When inherited through the female, the offspring are oedematous. When inherited through the male, the offspring show postnatal growth retardation.	Order
C3H-Crygs<Opj>/H	Crygs<Opj>	16	Opaque fibre cell junctions. Dominant cataract.	Order From EMMA
STOCK Opdc/H	Opdc	19	Optic disc coloboma. Mutants have retinal vascular abnormalities and optic discs of unusual size.	Order From EMMA
B6NDen;B6N-Orc5l<tm1 a(EUCOMM)Wtsi>/H	Orc5l<tm1a(EUCOMM)Wt si>	5		Order From EMMA
C3H101H-ostes/H	ostes	UN	Muscular dystrophy, small size and muscle wasting.	Order From EMMA
C.Cg-ostes/H	ostes	UN	Small with muscle tremor.	Order
P-Rex1 CE3/B6			Functional neutrophil deficiency	Order
B6J.129-S100A10<tm1J nw>/H	S100a10<tm1Jnw>	3	None.	Order From EMMA
B6;129P2-P2rx6<tm1Dg en>/H	P2rx6	16	No visible phenotype.	Order From EMMA
B6;129P2-P2ry12<tm1D gen>/H	P2ry12	3	None	Order From EMMA
129-Ncf1<tm1Hbd>/H	Ncf1<tm1Hbd>	5	Impaired innate immunity.	Order From EMMA
C3H101H-p<In(7p;Sox6 )100H>	Oca2<p-d>	7		Order
C3H101H-p<In(7p;Sox6 )100H>	In(7p;7Sox6)100H	7		Order
p<55H>	Tyr<c-ch>	7		Order
p<55H>	p<55H>	UN		Order
C3H101H-Oca2<p-61H>/ H	p<61H>	UN	p<61>/p slightly darker than p/p	Order
p<65H>	p<65H>	UN	Coat and eyes of p<65>/p darker than p/p. Coat and eyes of p<65>/p<65> only slightly lighter than wild-type.	Order
C3H101H-Oca2<p-66H>/ H	p<66H>	UN		Order
p<78H>	p<78H>	UN	p<78>/p looks like b/b. Coat and eyes of p<78>/p<78> only slightly lighter than wild type.	Order
Oca2<p-79H>	p<79H>	UN		Order
C3H101H-Oca2<p-80H>/ H	p<80H>	UN		Order
C3H101H-Oca2<p-81H>	Oca2<p-81H>	7	Phenotype of p<81H>/p is similar to p/p, homozygotes die pre-natally	Order
C3H101H-Oca2<p-82H>	Oca2<p-82H>	7	phenotype of p<82H>/p is similar to p/p, homozygotes die pre-natally	Order
p<83H>	p<83H>	UN		Order
C3H101H-Oca2<p-84H>	Oca2<p-84H>	7	phenotype of homozygotes is similare to p/p	Order
p<85H>	p<85H>	UN		Order
C3H101H-Oca2<p-86H>	Oca2<p-86H>	7	Phenotype similar to p/p	Order
p<87H>	p<87H>	UN		Order
p<87H>	p<d>	UN		Order
C3H101H-Oca2<p-88H>	Oca2<p-88H>	7	phenotype of homozygotes is similar to p/p	Order
p<91H>	p<91H>	UN		Order
p<92H>	p<92H>	UN		Order
C3H101H-Oca2<p-93H>/ H	p<93H>	UN		Order
p<95H>	p<95H>	UN		Order
C3H101H-Oca2<p-96H>/ H	p<96H>	UN		Order
p<97H>	p<97H>	UN		Order
C3H101H-Oca2<p-98H>/ H	p<98H>	UN		Order
C3H101H-Oca2<p-99H>/ H	p<99H>	UN		Order
C3H101H-Oca2<p-bs>/H	Oca2<p-bs>	7	p-black-eyed sterile	Order
p<cp>, p<bs>	Oca2<p-cp>	7	Coat colour same as p/p. p-black-eyed sterile, originally p<24>H,p<bs>/p<bs> viable but smallish, have slightly jerky behaviour, usually sterile & darker in colour than p<bs>/p<cp>, p<cp>/p<cp> usually die around birth from cleft palate, few have lived.	Order
p<cp>, p<bs>	Oca2<p-bs>	7		Order
p<d>, p<25H>	Oca2<p-d>	7	p<d>/p<d> eyes light at birth, dark at weaning. Coat similar to b/b but less "orange"	Order
p<d>, p<25H>	Oca2<p-25H>	7		Order
p<d>, p<6H>	Oca2<p-d>	7	p<d>/p<d> eyes light at birth, dark at weaning. Coat similar to b/b but less "orange"	Order
p<d>, p<6H>	Oca2<p-6H>	7		Order
STOCK Oca2<p-dn>/H	Oca2<p-dn>	7	Eyes pink at birth but darken by weaning. Coat slightly darker than p/p.	Order
C3H101H-Oca2<p-dn>/H				Order
C3H101H-Oca2<p-un>/H	Myo5a<d>	9	pink-eyed unstable	Order
C3H101H-Oca2<p-x>/H	Oca2<p-x>	7	Eyes dark at birth and weaning, coat only slightly lighter than wild type	Order
B6NDen;B6N-Pa2g4<tm1 a(EUCOMM)Wtsi>/H	Pa2g4<tm1a(EUCOMM)Wt si>	10		Order From EMMA
C3H-Paf/H	Paf	X	Patchy fur.	Order
B6;129P2-Pak2<tm1Dge n>/H	Pak2	16	None	Order From EMMA
C3H101H-Pax3<Sp-1H>	Pax3<Sp-1H>	1	splotch	Order
C3H101H-Pax3<Sp-2H>/ H	Pax3<Sp-2H>	1	splotch	Order From EMMA
C3H101H-Pax3<Sp-4H>	Pax3<Sp-4H>	1		Order
C3H101H-Pax3<Sp-5H>	Pax3<Sp-5H>	1	splotch	Order
C3H101H-Pax3<Sp-r>/H	Pax3<Sp-r>	1	splotch-retarded, spotting	Order From EMMA
Pax3<Sp>, Tyrp1<b-cH >	Pax3<Sp>	1	Splotch.	Order
Pax3<Sp>, Tyrp1<b-cH >	Tyrp1<b-cH>	4	Splotch.	Order
C3.D2-Pax6<Coop>/H	Pax6<Coop>	2	Heterozygotes have corneal opacity with iris anomaly and small eyes	Order
C3H;C-Pax6<Leca4>/H	Pax6<Leca4>	2	Mutants have small eyes, but not always corneal opacity (corneal opacity affects most other Pax6 mutants). Often have anterior cataract.	Order From EMMA
Pax6<Sey-Neu>	Pax6<Sey-Neu>	2	Small eye	Order
PC	a	2		Order
	Oca2<p>	7
	Tyr<c-ch>	UN
PCE/JP	a<t>	2		Order
	Sox18<Ra>	2
	Edn3<ls>	2
	Myo5a<d>	9
	Egfr<wa2>	11
	Wnt3a<vt>	11
C3H101H-Slc40a1<Pcm> /H	Slc40a1<Pcm>	1	Red ears and feet.	Order From EMMA
B6;129P2-Pde2a<tm1Dg en>/H	Pde2a	7	No visible phenotype.	Order From EMMA
B6;129P2-Pde3a<tm1Dg en>/H	Pde3a	6	No visible phenotype.	Order From EMMA
B6;129P2-Pde4b<tm1Dg en>/H	Pde4b	4	No visible phenotype.	Order From EMMA
B6;129P2-Pde4d<tm1Dg en>/H	Pde4d	13	No visible phenotype.	Order From EMMA
B6;129P2-Pde8a<tm1Dg en>/H	Pde8a<tm1Dgen>	7	No visible phenotype.	Order From EMMA
CBA/H-Pdss2<kd>/H	Pdss2<kd>	10	Kidney disease. Homozygotes develop nephrosis recognizable at about 10 weeks of age by drinking, loss of weight, anaemia, and death usually at 5 to 7 months.	Order
PED-JP/16				Order
C3H101H-Pedc/H			Pale ears, dark coat. Pre-implantation loss of homozygotes.	Order
PEDM/105			Elevated plasma phosphate.	Order
PEDM/14			Hyperglycaemia. Elevated plasma glucose at 16 and 24 weeks of age. No detection of glucose in the urine.	Order From EMMA
PEDM/15			High anxiety, tremors, small at weaning.	Order From EMMA
PEDM/25			This strain demonstrates late onset (>6 months of age) tremors and some individuals have a high nose-poking response in a behavioural test.	Order From EMMA
PEDM/29			Highly active and demonstrates a high degree of anxiety	Order From EMMA
PEDM/32			Albuminuria	Order
PEDM/35			Hyperglycaemia and glycosuria.	Order From EMMA
PEDM/36			Limb grasping, walks backwards, inactive	Order From EMMA
PEDM/41			Deformed digits shortened limbs	Order From EMMA
PEDM/42			Homozygotes have a belted white band of hair around the mouse middle. Their appearance is similar to that of the known mutation on Chromosome 15, Adamts20<bt> (Belted).	Order From EMMA
PEDM/83			Short/long faces and small mis-shapen eye sockets.	Order
PEDM52			Presumed homozygotes have spina bifida.	Order
PEDV/118				Order
PEDV/119				Order
PEDV/128				Order
PEDV/146			Dark skin in marble like patterns, slightly darker fur.	Order
PEDV/156			Headbob & head tilt.	Order
Pge<1H>	pge1<H>	UN		Order
C3H101H-pge<2H>/H	pge2<H>	UN		Order
C3H101H-Pge<3H>/H	pge3<H>	UN		Order
Pgk1<a>	Pgk1<b>	UN		Order From EMMA
Pgk1<a>	Pgk1<a>	UN		Order From EMMA
Pgm1<n1H>	Pgm1<c>	UN		Order
Pgm1<n1H>	Pgm1<n-H>	UN		Order
Pgm1<n2H>	Pgm1<n2H>	UN		Order
Pgm1<n2H>	Pgm1<c>	UN		Order
Pgm1<n3H>	Pgm1<n3H>	UN		Order
Pgm1<n3H>	Pgm1<c>	UN		Order
Pgm1<n4H>	Pgm1<n4H>	UN		Order
Pgm1<n4H>	Pgm1<c>	UN		Order
Pgm2<am>	Pgm2<am>	UN		Order
Pgm2<am>	Pgm2<a>	UN		Order
C3H101H-Ph/H	Ph	5	White 'belt'.	Order
C3H101H-Ph<3H>	Ph<3H>	5	patch	Order
STOCK Phex<Gy>/H	Gy	X	gyro	Order
STOCK Phex<Hyp>/H	Phex<Hyp>	X	hypophosphatemia	Order
Pk3<r>, Pk3<b>	Pkm2<a>	UN		Order
	Pkm2<b>	UN
	Pkm2<r>	UN
PKDBac Line2			Hets appear normal. Homs are small and develop hind-limb dragging at 4-6 weeks old	Order
C57BL/6Apb-Ikzf1<Pls tc>/Apb	Ikzf1<plstc>	11	Embryonic lethal E15.5-17.5. Anaemia. Failure of normal erythroblast growth & differntiation in feotal liver. Expansion of myeloid cells.	Order From EMMA
C3H;C-Play41/H	Play41	UN	Identified in circadian rhythm screen. Mutant mice demonstrate a long circadian period (24-24.5hr), and reduced activity.	Order From EMMA
C3H;C-Play50/H	Play50	UN	Identified in circadian rhythm screen. Reduced bouts of wheel- running activity	Order From EMMA
C3H;C-Play63/H			Reduced bouts of wheel- running activity.	Order From EMMA
C3H.Cg-Play1/H			These mice have a higher than normal degree of daytime activity in a 12:12 light:dark cycle.	Order From EMMA
C(C3)-Play16/H			No entrainment response to light pulses given at CT16.	Order From EMMA
PLAY19			Identified in circadian rhythm screen. Potentially no entrainment response to light pulses given at CT16	Order From EMMA
C3H.Cg-Play22/H	Play22	UN	Mice carrying this mutation show a low endurance of wheel running activity. Wheel running activity is about 10% of control animals.	Order From EMMA
C3H.Cg-Play31/H			Identified in a circadian rhythm screen. Wheel turning activity is dramatically reduced in a 12:12 light:dark cycle.	Order From EMMA
C3H;C-Play32/H			Identified in a circadian rhythm screen. These mice have reduced bouts of wheel running activity in a 12:12 light:dark cycle.	Order From EMMA
C3H;C-Play36/H	Play36	UN	Identified by circadian rhythm screen. Mutant mice demonstrate an increased phase shift after light pulse.	Order From EMMA
C3H;C-Play40/H			Identified in circadian rhythm screen. Mutants have potentially no entrainment response to light.	Order From EMMA
C3H;C-Play42/H			Identified in a circadian rhythm screen. These mice have two sets of activity onsets when first exposed to constant darkness conditions.	Order From EMMA
C3H;C-Play44/H			Identified in circadian rhythm screen. Potentially shows a large entrainment response to light and phase advancement in a 12:12 light:dark cycle.	Order From EMMA
C3H;C-Play46/H	Play46	UN	Poor entrainment to light in 12:12 light dark: cycle.	Order From EMMA
C3H;C-Play47/H			Identified in circadian rhythm screen. These mice free run in a 12:12 light:dark cycle.	Order From EMMA
C3H;C-Play57/H	Play57	UN	Identified in circadian rhythm screen. Mutant mice demonstrate a shorter cicadian wild type.	Order From EMMA
C3H;C-Play65/H			Changed period length after light pulse at CT16.	Order From EMMA
C3H;C-Play72/H			Reduced bouts of wheel running activity.	Order From EMMA
C3H;C-Play78/H			Potentially no entrainment response to light.	Order From EMMA
C3H;C-Play79/H			Poor entrainment response to light.	Order From EMMA
C3H;C-Play81/H			Long circadian period & poor entrainment response	Order From EMMA
C3H;C-Play82/H			This mutation was identified in a circadian rhythm screen. It shows reduced bouts of wheel-running activity.	Order From EMMA
Plcg2<tm>-383/Bcl2-3 6Tg	Plcg2	8	B cell dysfunction. Homozygotes are infertile.	Order From EMMA
ple			Pale.	Order
C3H101H-Plp1<jp-rsh> /H	Plp1<jp-rsh>	X	Shivering/shaking of hind quarters.	Order
GENA300			Late onset deafness	Order From EMMA
POMC-Cre				Order
Pomc-cre Z/EG				Order
B6;129P2-Prep<tm1Dge n>/H	Prep	10	None	Order From EMMA
129P2/OlaHsd-Prnp/Pr nd<tm1Dwm>/H	Prnp/Prnd<tm1Dwm>	2	No phenotype in female mice. Male homozygotes are sterile.	Order
Prnp<a(108L_189V)> (DD)			No phenotype	Order
Pro-Cre			None.	Order From EMMA
PrP Chicken-repeats	Prnp<tm1Cwe>	2	The octameric repeat region of the mouse prion protein was replaced with the hexameric repeat region from the domestic chicken. The mice express mouse PrP at wild-type levels with correct membrane location and orientation but have an altered metal binding region. The mice have been generated to get a better understanding of prion diseases such as CJD in humans.	Order From EMMA
Ps	Tyrp1<b>	UN	Syndactyly, extra digit, webbing of soft tissue on feet.	Order
Ps	a<e>	UN	Syndactyly, extra digit, webbing of soft tissue on feet.	Order
PT	Tyr<c-ch>	7		Order
	Ednrb<s>	14
	Myo5a<d>	9
	Tyrp1<b>	4
	Bmp5<se>	9
	Oca2<p>	7
PTP/H	Myo5a<d>	9		Order
	Tyrp1<b>	4
	Gpi1<a>	7
	Tyr<c-ch>	7
	Hbb<s>	7
	Bmp5<se>	9
	Ednrb<s>	14
	a	2
	Oca2<p>	7
	Car<2b>	UN
	Pgm1<b>	UN
	Hba<f>	UN
	Es3<b>	UN
B6;129-Ptprc<tm1Holm >/H	Ptprc<tm1Holm>	1	Defective lymphocyte development, more severe in T lineage, severe combined immunodeficiency.	Order From EMMA
C3H101H-Wnt7a<px>/H	Wnt7a<px>	6	Sterility. Skeletal abnormalities, mainly forelimb abnormalities. Postaxial hemimelia, recessive. The forelimbs are regularly affected. There may be absence of digits 5, 4, and 3, & reduction or absence of the ulna. There is always a large oval foramen in the scapula. The hindlimbs are usually normal, but digit 5 may be absent, and occasionally the fibula is reduced. Mice with severally affected limbs tend to have an extra pair of ribs and a slight reduction in number of presacral vertebrae. Both sexes are sterile and show anomalies of the Mullerian ducts, including a partly or wholly double vagina and uncoiled oviducts in the female, and peristent Mullerian ducts in the male.	Order From EMMA
Qk<qk>	Qk<qk>	17	Homozygotes shake and tremble when walking. Males sterile.	Order
Quaver			Tremors.	Order
STOCK Rb(4.6)2Bnr-Rb (4.15)4Rma-Rb(6.15)1Ald-Adamts20<bt>/H	Adamts20<bt>	15		Order
STOCK Rb(4.6)2Bnr-Rb (4.15)4Rma-Rb(6.15)1Ald-Tyrp1<B-lt>Adamts20<bt>/H	Adamts20<bt>	15		Order
	Tyrp1<B-lt>	4		Order
STOCK Rb(2.8)6Rma-Rb (6.15)1Ald-Rb(9.19)163H/H				Order
STOCK Rb(1.15)2Ct Rb (2.18)6Rma Rb(6.13)3Rma Rb(11.16)2H/H				Order
rag1<tm1ES>	Rag1	2		Order
C3H;C-Rasgrf1<enu2H> /H	Rasgrf1<enu2H>	9	Small.	Order From EMMA
STOCK Rb(1.10)10Bnr				Order
Rb(1.15)2Ct ln				Order
STOCK Rb(1.2)5H				Order
STOCK Rb(1.3)1Bnr				Order
STOCK Rb(10.11)8Bnr			Heterozygous females give low frequencies of aneuploid fetuses	Order
STOCK Rb(11.13)4Bnr			Testis weight reduced in both homozygotes and heterozygotes.	Order
STOCK Rb(11.16)2H				Order
C3H101H-Rb(12.13)3Ct				Order
STOCK Rb(16.17)7Bnr			Reduced testis weight in homozygotes.	Order
STOCK Rb(16.19)1Bu/H				Order
STOCK Rb(2.17)11Rma				Order
STOCK Rb(2.17)4H				Order
STOCK Rb(2.18)6Rma				Order
C3H101H-Rb(4.14)8H				Order
STOCK Rb(4.15)4Rma				Order
C3H101H-Rb(4.16)10H				Order
STOCK Rb(4.18)3H				Order
STOCK Rb(4.6)2Bnr				Order
Rb(4.6)2Bnr, Rb(9.14 )6Bnr	Bmp5<se>	9		Order
	Tyrp1<b>	4
	Tgfa<wa1>	6
	Myo5a<d>	9
	Ednrb<s>	14
STOCK Rb(5.15)3Bnr/H				Order
STOCK Rb(5.19)1Wh				Order
STOCK Rb(6.13)1H				Order
C3H101H-Rb(6.13)3Rma				Order
STOCK Rb(6.15)1Ald				Order
C3H101H-Rb(8.12)5Bnr			testis weight are reduced in both homozygotes and heterozygotes and the sperm count for the former is significantly lower	Order
Rb(8.19)1Ct				Order
STOCK Rb(9.14)6Bnr			Testis weights are reduced in both homozygotes and heterozygotes and sperm count compared to control males was approximately halved in the former.	Order
STOCK Rb(9.19)163H				Order
C3H101H-Rb(X.12)7H			Heterozygous females are fertile but hemizygous males are sterile	Order
STOCK Rb(X.2)2Ad				Order
STOCK Rb(X.9)6H				Order
C3H;C-Rky/H	Rky	UN	At 10 weeks of age, pups show a swim phenotype described as rocky, leaning and jerky. By 18 weeks of age mice develop a head-bobbing/circling cage phenotype.	Order From EMMA
REC/9			Weak limb grasp, belly spot.	Order From EMMA
RECB/13			Single fetus observed with severe neural tube defect; possibly polygenic defect	Order From EMMA
C3H.Cg-Tulp3<hhkr>/H	Tulp3<hhkr>	6	Homozygotes have spina bifida and oedema, and die at birth.	Order
Steap<Fred>	Steap3<fred>	1	Abnormalities in red blood cell size and shape.	Order From EMMA
Redeye			Homozygous mutant mice exhibit a range of eye defects including pale retinas, vascular defects & white structures present in the eye.	Order
RegIII Beta knockout			none	Order From EMMA
STOCK Mitf<Rorp>/H	Mitf<Rorp>	6	Dilute coat/ear/tail colour. Heterozygotes have pigment dilution, while homozygotes lack coat pigment, but retain eye(iris) pigment and do not have small eyes.	Order From EMMA
STOCK Rvm/H	Rvm	14	Retinal vascular abnormalities.	Order From EMMA
STOCK Rwhs/H	Rwhs	11	Retinal white spots. In heterozygotes, white spots appear on the retina from one month of age. They do not seem to reduce vision.	Order From EMMA
B6;129P2-Rgs5<tm1Dge n>/H	Rgs5<tm1Dgen>	1	No visible phenotype.	Order From EMMA
C3H101H-Ri/H			Ringed.	Order
Ricky				Order
RIII/Dk	Prn-i<n>	UN		Order
RKS-XI			No overt phenotype. Believed to be a silent mutation of Pkd111.	Order
STOCK Rn/H	Rn	14	Rn heterozygotes have white or partly pigmented hairs throughout coat. Homozygotes are lighter than heterozygotes and are viable and fertile	Order
STOCK Rn<fkl>	Rn<fkl>	14	freckled	Order
B6NDen;B6N-Rnf7<tm1a (EUCOMM)Wtsi>/H	Rnf7<tm1a(EUCOMM)Wts i>	9	Full description available in Europhenome	Order From EMMA
C3H;C-Aff1<Rob>/H	Aff1<Rob>	5	Robotic and jerky gait. Heterozygotes exhibit small size, ataxia, adult-onset Purkinje cell loss, cataracts, reduced survival, and low fertility.	Order From EMMA
ROHi			Long term growth selected mouse line.	Order
ROLi			Long term growth selected lines.	Order
C3H101H-rst/H	rst	UN	rosette	Order
C3H101H-Hps5<ru2>	Hps5<ru2>	7	ruby-eye	Order
C3H101H-Rw/H	Rw	5	Rw (rump-white) is homozygote lethal. Heterozygotes have white hindlegs and tails and white fur on the posterior part of the abdomen.	Order From EMMA
Rw,Kit<W-bd>	Kit<W-bd>	5	No pigment in rump area	Order
	Kit<W-v>	5
	Rw	5
S1.2DEL			Loss of Igf2 imprinting.	Order From EMMA
S1.2NEO			Intra-uterine growth restriction (paternal transmission).	Order From EMMA
sa mu	Muted<mu>	13	sa: silky coat with a high sheen, mu/mu have fur of a muted brown colour.	Order
sa mu	Foxq1<sa>	13		Order
sa mu pe	Foxq1<sa>	13	satin, muted, pearl stock.	Order
	Muted<mu>	13
	Ap3b1<pe-H>	UN
SAA2			None.	Order From EMMA
C3H;C-Sagg/H	Sagg	1	Heterozygotes have loose skin.	Order From EMMA
C57BL/6Apb-Rc3h1<san >/Apb	Rc3h1<san>	1	Autoimmune disease, ANA, lymphadenopathy, splenomegaly, hyper IgG, SLE.	Order From EMMA
SB1			Reduced hearing by clickbox.	Order
SB2/1			Reduced hearing	Order From EMMA
C3H101H-Sby<2H>/H			Curly whiskers/absent at birth. Sporadic lack of fur growth.Some growth retardation from birth	Order From EMMA
C3H101H-scb/H	scb	8	Scabby.	Order
STOCK Scr/H	Scr	6	Scruffy.	Order
B6;129P2-Scube3<tm1D gen>/H	Scube3	17	No visible phenotype.	Order From EMMA
SCW			Severe immunodeficiency.	Order
STOCK Sd/H	Sd	2	Urogenital abnormalities	Order
SDL	Myo5a<d-l>	9	Dilute coat. The colour of d<l>/ d<l> is identical to that of d/d but the mice develop a severe neuro-muscular disorder characterised by convulsions and opisthotonas (arching upwards of the head and tail) and they die at about 3 weeks.	Order
	Bmp5<se>	9
	Myo5a<d>	9
C3H;C-Sbc/H	Sbc	16	Identified in circadian rhythm screen. These mice change their period length from normal to long after a light pulse is given at CT16 (circadian time).	Order From EMMA
C3H;C-Heph<Sla>/H	Heph<Sla>	X	Heterozygous females have striped coats. Males are small and pale at birth and most die within 1 week of birth. Females are classed at 8 days of age. Sla is an X linked dominant and classed as a harmful mutant due to lethality of males.	Order From EMMA
C3H101H-Pax6<Sey-3H>	Pax6<Sey-3H>	2	Small at birth and weaning with small eyes, white feet and sometimes a belly spot	Order
C3H101H-Pax6<Sey-H>	Pax6<Sey-H>	2	Small-eye.	Order From EMMA
129-Foxp3<sf>/H	Foxp3<sf>	X	scurfy, scaliness first of tail later other parts of body, skin tight, eyelids open late, males usually die before / shortly after weaning, survivors small & sterile, small abdominal tetsis & lack scrotum. Occasional sf females are X/O resemble sf males. Similar human disease: Ichthyosis and Male Hypogonadism	Order From EMMA
C3H;C-Sfrp2<C50F>/H	Sfrp2<C50F>	3	Normal.	Order
B6J.Cg-Sfrp2<l153N>/ H	Sfrp2<I153N>	3		Order
B6J.Cg-Sfrp2<l153N>/ H			No Overt Phenotype. Full description available from Europhenome	Order
B6.Cg-Sfrp2<C50F>/H	Sfrp2<C50F>	3		Order
B6.Cg-Sfrp5<Q27STOP> /H	Sfrp5<Q27stop>	19		Order
Sgd			Small at birth and weaning, progressive hairless (from 3 weeks of age) with accompanying thickinening of the skin	Order
Shby/+			Shabby. Patchy coat, tail rough. Cyclic epilation.	Order
Sherbert				Order
C3H.Cg-Sfl/H	Sfl	2	Identified in circadian rhythm screen. Mice carrying this mutation have no phase shifting response to a light pulse given at CT16.	Order From EMMA
C3H.Cg-Sci/H	Sci	8	Identified in circadian rhythm screen. Short circadian period of wheel-running activity (22.5 hrs rather than 23.5 hrs). Wheel running activity is about 10% of control animals.	Order From EMMA
Shp2CS x DO11.10 L1			Characterisation of the phenotype is still in progress, but the line displays amplified cytokine secretion in response to antigenic challenge	Order
Shp2CS x DO11.10 L5			Characterisation of the phenotype is still in progress, but the line displays amplified cytokine secretion in response to antigenic challenge	Order
Shp2CSxB10.BR Line 1			Characterisation of phenotype still in progress but line displays defective primary immune responses to T-dependent antigen and amplified cytokine secretion in response to antgenic challenge.	Order From EMMA
C3H;C-Sic/H	Sic	7	Sickly . Classed as harmful. Heterozygotes are small and sickly. Mutation has not been tested for homozygosity. The Sickly mice are marginally smaller than wildtype sibs at birth and dramatically smaller (<50%) at weaning. The nature of this growth defect has yet to be investigated. Heterozygous mice are also prone to infection.	Order From EMMA
SIG (Position Testin g Stock chr.6)	Grid2<Lc>	6	Mitf<Mi-wh> is semidominant. The homozygotes are viable white mice, the eyes are pink at birth. The heterozygotes have light sandy coats and belly spots. Grid2<Lc> is homozygous lethal, the heterozygotes have swaying hindquarters and jerky up and down movement. Sig is homozygous lethal, the heterozygotes are blind, the eyes are open at birth, some exhibit hydrocephaly.	Order
	Mitf<Mi-wh>	6
	Sig	6
C3H101H-skimp/H	skimp	7		Order
C3H;C-Jag1<Slalom>/H	Jag1<Slalom>	2	These mice exhibit head weaving and shaking behaviour.	Order From EMMA
Slc38a4<tm2Kel>/Delt aCG1A			None, a minor effect on term weight.	Order From EMMA
B6;129P2-Slc7a10<tm1 Dgen>/H	Slc7a10<tm1Dgen>	7	No visible phenotype.	Order From EMMA
C3H101H-Pou3f4<Slf>/ H	Pou3f4<Slf>	X	sex-linked fidget	Order
Slip				Order
C3H.Cg-Sgh/H	Sgh	4	Mice carrying this mutation demonstrate a low endurance of wheel running activity which is reduced to about 10% of control values.	Order From EMMA
Smad 2 D2			None	Order From EMMA
Smad 2 FL	Smad2	18	Embryonic lethal at day 8.5 dpc.	Order From EMMA
Smad 2 SF	Smad2	18	Homozygous lethal at day 8.5.	Order From EMMA
Smad 2 T3	Smad2	18	Approx 50% of homozygotes are embryonic lethal at 15d, remainder are viable as adults.	Order From EMMA
Smad8 conditional			None	Order From EMMA
Smad8 LacZ	Smad9<tm1Rob>	3	None	Order From EMMA
C3H101H-Sme/H	Sme	UN	Reduction in size of pinna and often irregular in shape	Order
SMN E134K Transgenic			None.	Order From EMMA
SMN2 low	Tg(SMN2)89Ahmb	UN	Mice that are homozygous for the targeted mutant Smn1 allele and carry the SMN2 transgene exhibit symptoms and neuropathology similar to patients afflicted with type I proximal spinal muscular atrophy (SMA) but die at P6. (See Monani 2000 HMG 9 333-339). Mice homozygous for Smn1-/-, in the absence of SMN2 would die before birth. Heterozygotes for the knockout show no phenotype.	Order
SMN2 low	Smn1<tm1Msd>	13		Order
SMNDelta5			None.	Order From EMMA
SMNDelta5-SMN2Low			Rescues post natal lethality of SMN2 low strain	Order From EMMA
SOCS-6	Socs6<tm1Dlk>	18	10% increased body weight & increased insulin sensitvity.	Order From EMMA
sooty foot	soo	2		Order
Sox4<m91Ark>	Sox4<m91Ark>	13	Embryonically lethal.	Order From EMMA
GENA203			Polydactyly.	Order From EMMA
C3H.Cg-Celsr1<Scy>/H	Celsr1<Scy>	15	Mice carrying this mutation exhibit circling behaviour.	Order From EMMA
C57BL-Spnb4<qv-3J>/H	Spnb4<qv-3J>	7	Heterozygotes apppear normal, homozygotes have locomotor instability, pronounced quivering, deafness. Homozygote males are sterile.	Order
Ssm			shaker small	Order
Ssy			small syndactyly	Order
C3H101H-Nsdhl<Str-1H >/H	Nsdhl<Str-1H>	X	striated	Order From EMMA
C3H101H-Nsdhl<Str-2H	Nsdhl<Str-2H>	X	striated	Order
C3H;C-Strg/H	Strg	X	Striped and greasy.	Order
STOCK Sts<->/H				Order
STOCK Myo6<sv>/H	Myo6<sv>	9		Order
Svc (GENA 291)	Col4a1<Svc>	8	Small with vacuolar cataract	Order
C3H101H-Dync1h1<Swl> /H	Dync1h1<Swl>	12	Sprawling, abnormal posture and locomotion from defective position sense mainly affecting hind limbs, myelination deficient, deficiency of sensory receptors, spindles virtually absent from hind limbs.	Order From EMMA
SWR/Ola Hsd	Tyr<c>	7		Order
Sxr	Eda<Ta-33H>	X		Order
C3H101H-Tp(Y)1Ct<Sxr -b>/H	Tp(Y)1Ct<Sxr-b>	Y		Order
sy<a>			Shaker with syndactylism Albany.	Order
B6;129-Sycn<tm1Rja>/ H	Sycn<tm1Rja>	7	Pancreatic secretion compromised.	Order From EMMA
C3H101H-T(10;13)199H				Order
C3H101H-T(10;18)18H				Order
T(10;18)18Hdl				Order
C3H101H-T(11;13)41Ad				Order
T(11;13)41Ad cross 2				Order
C3H101H-T(11;13)56H				Order
C3H101H-T(11;19)42H				Order
C3H101H-T(13;14)69H				Order
T(14;15)6Ca hr				Order
CBA/H-T(14;15)6Ca				Order
T(1;10)73H				Order
C3H101H-T(1;12)52H				Order
STOCK T(1;13)70H				Order
JUN-T(1;2)5Ca				Order
C3H101H-T(1;4)71H				Order
C3H101H-T(1;6)42Ad				Order
C3H101H-T(1;7)49H				Order
C3H101H-T(1;8)63H				Order
C3H101H-T(2;11)30H				Order
T(2;11)30H - cross 4				Order
C3H101H-T(2;14)48H				Order
C3H101H-T(2;15)45Ad/ H				Order
STOCK-T(2;16)28H				Order
STOCK-T(2;19)68H				Order
C3H101H-T(2;3)24H				Order
C3H101H-T(2;4)13H				Order
C3H101H-T(2;4)1Ca				Order
T(2;4)1Go				Order
STOCK T(2;4)1Sn				Order
T(2;5)72H				Order
C3H101H-T(2;6)7Ca				Order
T(2;8)26H				Order
STOCK T(2;8)2Wa/H				Order From EMMA
T(2;9)11H				Order
C3H101H-T(3;10)61H				Order
C3H101H-T(3;12)58H				Order
C3H101H-T(3;19)25Ad				Order
C3H101H-T(3;8)56Ad				Order
C3H101H-T(4;10)Hsc76 H/H			Head shaker, circling.	Order
C3H101H-T(4;12)47H				Order
C3H101H-T(4;5)46H				Order
C3H101H-T(4;6)77H/H			Homozygotes are sometimes infertile.	Order
C3H101H-T(4;6)77H-Mi tf<Mi-wh>/H	Mitf<Mi-wh>	6	Homozygotes sometimes infertile.	Order
T(4;8s)36H				Order
STOCK T(4;9)45H				Order
C3H101H-T(5;11)57H			Semi-sterile.	Order
C3H101H-T(5;12)31H				Order
STOCK T(5;13)264Ca				Order
C3H101H-T(5;7)30Ad				Order
C3H101H-T(6;12)32H				Order
C3H101H-T(6;13)6Ad				Order
T(6;14)39H				Order
STOCK T(6;7)51H				Order
C3H101H-T(6;8)2Ad				Order
STOCK T(7;11)40Ad/H				Order
STOCK T(7;11)65H			Reciprocal translocation	Order
C3H101H-T(7;13)7Ad				Order
C3H101H-T(7;15)9H			Heterozygotes are semi-sterile.	Order
C3H101H-T(7;16)67H				Order
STOCK T(7;19)145H			Male sterile.	Order From EMMA
C3H101H-T(9;10)62H				Order
STOCK T(9;17)138Ca				Order
C3H101H-T(In1;5)44H				Order
C3H101H-T(X;11)38H				Order
C3H101H-T(X;4)37H				Order
STOCK T(X;7)3Neu				Order
C57BL/6Apb-Lcp2<twm> /Apb	Lcp2<twm>	11	Few naïve CD4+ and CD8+ T cells, autoimmunity, 5fold decrease in DP Tcells. Defects in positive selection & reduced negative thymocyte selection, hypergammaglobulinemia and hyper-IgE.	Order From EMMA
STOCK T<21H>/H	T<21H>	17	Effects like brachyury	Order From EMMA
C3H101H-T<22H>	T<22H>	17	T<22H>/t<6> males have enhanced transmission ratio	Order
C3H101H-T<24H>/H	T<24H>	UN	Brachyury.	Order
C3H101H-T<25H>/H	T<25H>	UN	brachyury, sometimes slightly small mice with shortened, kinky tails. Males breed satisfactorily but females show impaired transmission producing few T<25H> offspring which have low viability. Homozygote presumed lethal.	Order
T<26H>	T<26H>	UN	brachyury	Order
C3H101H-T<29H>	T<29H>	17		Order
C3H101H-T<30H>	T<30H>	17		Order
C3H101H-T<31H>	T<31H>	17	Short tails	Order
C3H101H-T<32H>/H	T<32H>	17	Heterozygotes - short tail, homozygotes - lethal.	Order
C3H101H-T<33H>	T<33H>	17	short tails. Homozygotes lethal.	Order
C3H101H-T<34H>	T<34H>	17	Heterozygotes - short tail, Homozygotes - lethal.	Order
C3H101H-T<36H>	T<36H>	17	Short tails	Order
STOCK t<6>/H	t<6>	17	Taillessness with T	Order
C3H101H-T<c-2H>	T<c-2H>	17	tailless	Order
C3H101H-T<c>/H	T<c>	17	T<c>/+ and T<c>/t<h7> tailless. T<c>/T<c> lethal, like T/T but more severely affected	Order From EMMA
C3H101H-t<h17>	t<h17>	17		Order
t<h18> t<h2>	t<h18>	17	Gives tailless with T. Homozygotes for t<h18> are lethal. t<h18> carries distal distortion D2 and t<h2> carries responder R.	Order
t<h18> t<h2>	t<h2>	17		Order
STOCK t<h20>	t<h20>	17		Order
STOCK t<h44>	t<h44>	17	T/t<h44> tailless	Order
STOCK t<h49>	t<h49>	17		Order
STOCK t<h50>	t<h50>	17		Order
STOCK t<h51>	t<h51>	17		Order
t<h51>t<h18>	t<h18>	17	Lethal when homozygous.	Order
	t<h51>	17
	t<lowH>	17
C3H101H-t<h57>	t<h57>	UN		Order
STOCK t<h7>	t<h7>	17		Order
t<h7m2>	t<h7m2>	UN	tailess with T	Order
t<h7m>	t<h7m>	UN	Tailless with T, homozygous viable.	Order
t<h7m>	T<21H>	UN	Tailless with T, homozygous viable.	Order
STOCK T<hp>/H	T<hp>	17		Order
t<hr15>	t<hr15>	UN	Tailess	Order
t<hr1>	t<hr1>	UN	Tailless	Order
t<hr4>	t<hr4>	UN	Tailless	Order
t<low2H>	t<low2H>	UN		Order
t<low3H>	t<low3H>	17		Order
STOCK t<lowH>	t<lowH>	17		Order
STOCK t<lowH>	t<low2H>	UN		Order
STOCK t<lub2>/H	t<Lub2>	17		Order
STOCK t<s6>/H	t<s6>	17		Order
STOCK t<w32>/H	t<w32>	17		Order
C3H101H-t<w32m>/H	t<w32m>	UN		Order
t<x507>	t<x507>	UN	Tailess	Order
t<x507>	tf<t>	UN	Tailess	Order
Ta<10H>	Eda<Ta-10H>	UN	Tabby.	Order
C3H101H-Eda<Ta-23H>	Eda<Ta-23H>	X		Order
Ta<23H> Xce<c> Pgk1< a>	Eda<Ta-23H>	X		Order
	Xic<c>	X
	Pgk1<a>	UN
C3H101H-Eda<Ta-25H>	Eda<Ta-25H>	X	tabby	Order
C3H101H-Eda<Ta-26H>	Eda<Ta-26H>	X	tabby, has a hairy tail	Order
C3H101H-Eda<Ta-27H>/ H	Eda<Ta-27H>	UN	Tabby. The males have hairless tails.	Order
C3H101H-Ta<28H>/H	Eda<Ta-28H>	UN	Tabby. The males have hairless tails.	Order
C3H101H-Eda<Ta-29H>	Eda<Ta-29H>	X	tabby, males have hairless tails	Order
C3H101H-Eda<Ta-30H>	Eda<Ta-30H>	X	tabby	Order
C3H101H-Eda<Ta-32H>	Eda<Ta-32H>	X	tabby	Order
C3H101H-Eda<Ta-33H>	Eda<Ta-33H>	X	tabby, hairy tail and the teeth do not need cutting	Order
C3H101H-Ta<35H>/H	Eda<Ta-35H>	UN	Tabby, males have hairless tails and are bald behind the ears.	Order
C3H101H-Eda<Ta-36H>/ H	Eda<Ta-36H>	UN	Tabby.	Order
Ta<37H>	Eda<Ta-37H>	UN	tabby	Order
C3H101H-Eda<Ta-38H>/ H	Eda<Ta-38H>	UN	Tabby.	Order
C3H101H-Eda<Ta-39H>/ H	Eda<Ta-39H>	UN	Tabby.	Order
Ta<44H>			TA<Fa> like ie heterozygous females-striped, Hemizygous males-weak teeth, no guard hairs, bald tails, very little hair behind ears.	Order From EMMA
C3H101H-Tal/H	Tal	14	Heterozygotes cannot easily be identified at birth but can be classified at weaning. The feet are held in an abnormal position, there is soft tissue syndactylism involving digits 2,3, and to a lesser degree 4, and there is often overgrowth and twisting of the toenails. The forefeet are less obviously affected than the hindfeet. Homozygotes are more severely affected with extreme shortening of the phalanges and significant reduction to the metatarsals. The tail shows a kinking to form a hook near the tip.	Order
TAS16			Curly tail	Order From EMMA
TAS2			Belly spot, head spot, white feet (variable).	Order From EMMA
TAS4			Multiple white spotting over entire body	Order From EMMA
TAS6			Belly spot, white feet, head spot	Order From EMMA
tcl<6>	tcl<6>	UN		Order
Tcx			Striped coats in females,greasy coat in males.	Order
C3H101H-Ebp<Td>/H	Ebp<Td>	X	Tattered.	Order From EMMA
tde	Grxcr1<pi-tde>	5	insertional mutation Tasmanian devil	Order
TERB-54			Possible modifier of Huntingdon's disease. Affected mice present with gait problems.	Order
TERB-56			Possible modifier of Huntingdon's Disease. Affected mice have intermittent paralysis in one hind leg. Culled at 12 weeks	Order
TERB-57				Order
C3H101H-Tesa/H	Tesa	UN	Mice carrying this mutation are deaf, have short tails and exhibit circling behaviour.	Order From EMMA
TESOD-20			This stock is a model for ALS (Amyotrophic Lateral Sclerosis), a progressive, usually fatal neurogenerative disease caused by the degeneration of motor neurons. They are carrying a modifier ENU induced mutation that makes their whole phenotype more severe. Mice were dying at around 30-35 weeks of age with a severe ALS phenotype so therefore they are usually humanely killed once they get one hind limb paralysed.	Order
Tesod-36				Order
TESOD-37				Order
TFH				Order
TFH/H	T	17	Shorter tail, blunt.	Order From EMMA
TFH/H	tf	17	Shorter tail, blunt.	Order From EMMA
TFL				Order
C3H101H-Cacna1a<tg>/ H	Cacna1a<tg>	8	Tottering phenotype. Homozygotes have wobbly gait from 3-4 weeks and intermittant seizures. Heterozygotes appear normal.	Order
Tg(-214VpreB1-huCD12 2)F133Lmb			No known effects	Order From EMMA
Tg(5'lambda 5-huCD25 )82Lmb			No known effects	Order
Tg(CMV-tetO-CFTR)TC3 5CH			None	Order From EMMA
Tg(Leftb-cre)1Hmd	Tg(Leftb-cre)1Hmd	UN		Order
Tg(Nmnat1) 7104Cole			None.	Order
B6J;CBA-Tg(RP1-309F2 0)48Kel				Order From EMMA
Tg(RP21-340H11)29Kel			Mild hyperglycaemia in neonates, mildly impaired glucose tolerance post weaning.	Order From EMMA
CBB6-Tg(runx1/MTG8)I CH10Fc/H				Order
CBB6-Tg(runx1/MTG8)I CH11Fc/H				Order
CBB6-Tg(runx1/MTG8)I CH12Fc/H				Order
CBB6-Tg(runx1/MTG8)I CH7Fc/H				Order
CBB6-Tg(runx1/MTG8)I CH8Fc/H				Order
CBB6-Tg(runx1/MTG8)I CH9Fc/H				Order
Tg(Sox2-cre)1Amc	Tg(Sox2-cre)1Amc	UN		Order
Tg(T-cre)1Lwd	Tg(T-cre)1Lwd	UN		Order
Tg(TH1-TauV337m)T39	Tg(Thy1-MAPT*V337M)1 Godt	UN	Development of abnormal tau phosphorylation & aggregation within the brain, as seen in Alzheimer's & other tauopathies. Highly discrete & specific age-dependent cognitive changes including memory impairment & impaired impulse control.	Order
Tg(Wnt1-cre)11Rth	Tg(Wnt1-cre)11Rth	UN		Order
129-Tgfbr2<tm1Roes>/ RoesH	Tgfbr2<tm1Roes>	9		Order From EMMA
STOCK Epo<Tg(SV40T/E po)134.3LCPjr>/H	Epo<Tg(SV40T/Epo)134 .3LCPjr>	UN	Homozygotes have incomplete epo deficiency and are anaemic.	Order From EMMA
Tg(bTGTRfs)1Vkc				Order
TgN(CEB1GEN)-G			None	Order
TgN(CEB1GEN)-H			None	Order
TgN(CEB1GEN)-I			None	Order
B6C3-Tg(HD82Gln)81Db o/H	Tg(HD82Gln)81Dbo	UN	Onset of abnormal gait and tremors at 3 months. Fail to gain weight from 2 months.	Order
B6CB-Tg(PMP22)C1Clh	Tg(PMP22)C1Clh	UN		Order
B6;CB-Tg(PMP22)C22Cl h/H	Tg(PMP22)C22Clh	UN	Shaking & unsteady gait.	Order From EMMA
B6CB-TgN(PMP22)C58Cl h				Order
B6CB-Tg(PMP22)C61Clh				Order
B6CB-Tg(PMP22)JP18Cl h				Order
(B6xCB)F2-Tg(PMP22)M Y41Clh	Tg(Pmp22)My41Clh	UN	Shaky & unsteady gait.	Order
B6CB-Tg(pUHG16)JU2Cl h			None	Order
B6CB-Tg(yCFTR)A10Clh /H			None	Order
B6CB-Tg(yCFTR)T30Clh /H				Order
B6CB-Tg(yCFTR)T57Clh /H			None.	Order
TgNmnat1 line 881			None.	Order
C57BL/6S-Hnrpll<thdr >/Apb	Hnrpll<thdr>	17	A marked reduction in the no. of peripheral T cells, especially naïve CD4 & CD8 cells, and poor survival of thunder T cells upon adoptive transfer. The T cells are hyperactivated.	Order From EMMA
Tiffany			Mice exhibit eye defects. Sections of the lens diffract light differently.	Order
C57BL/6Apb-Lig4<tiny >/Apb	Lig4<tiny>	8	Small in size, no CD8 cells or B cells, TCR Tg appears to rescue T cells. Similar to human SCID.	Order From EMMA
Tis11b<tm1mt>			Day 9 embryonic lethal	Order
C3H101H-Tks/H	Tks	9	tail kinks	Order
B6;129P2-Tln1<tm1Cri t>/CritH	Tln1<tm1Crit>	4		Order From EMMA
129/SvEv-Tln1<tm1Cri t>/CritH	Tln1<tm1Crit>	4		Order
Tlss			Thymo lymph sarcoma susceptibility.	Order
TM/45			Abnormal response to Intraperitoneal Glucose Tolerance Test at 24 weeks of age.	Order From EMMA
TM/47			Mutant mice fail to bury marbles in sawdust when left for a period of 30 minutes.	Order From EMMA
TM/58			These mice have an abnormal walking posture, appearing as though the hips are fused. Histological examination shows this to be a muscular phenotype.	Order From EMMA
TM/59			Abnormal response to Intraperitoneal Glucose Tolerance Test at 12 weeks of age. Fasting hyperinsulinaemia at 16 weeks. Mice are significantly heavier than wildtype at 12 and 16 weeks of age.	Order From EMMA
TM/60			Abnormal response to Intraperitoneal Glucose Tolerance Test at 12 weeks of age. Abnormal IPGTT and fasting hyperinsulinaemia at 16 weeks. Mice are significantly heavier than wildtype at 12 and 16 weeks of age.	Order From EMMA
TM13			Head bobbing	Order From EMMA
TM2			Behavioural/low anxiety phenotype	Order
TM4			High T60 in intraperitoneal glucose tolerance tests.	Order From EMMA
B6;129P2-Tmem67<tm1D gen>/H	Tmem67	4	No visible phenotype	Order From EMMA
TMR/10			Mutant mice fail to bury marbles in sawdust when left for a period of 30 minutes.	Order From EMMA
Tmsb4x<tm1Tnr>	Tmsb4x	X	B-cell defect.	Order From EMMA
To	Cat5<To2>	10		Order
C3H101H-Lim2<To3>/H	Lim2<To3>	7	Total opacity, dominant cataract.	Order From EMMA
B6;129P2-Tpcn1<tm1Dg en>/H	Tpcn1	5	No visible phenotype. IVF/1772.1k - short tail, IVF/1772.1m- tail kink.	Order From EMMA
TPL				Order
Tpm1<tm1aWtsi>	Tpm1	9	None.	Order From EMMA
C3H.Cg-Pmp22<Tr-1H>/ H	Pmp22<Tr-1H>	11	Tremors with seizures. Tremors, muscle weakness.	Order From EMMA
C3H;C-Pmp22<Tr-2H>/H	Pmp22<Tr-2H>	11	Tremors, muscle weakness.	Order From EMMA
Trembly			Muscular dystrophy, small size, muscle wasting.	Order
C3H101H-Trf<bm>/H	Trf<bm>	UN		Order
B6;129P2-Trpc4<tm1Dg en>/H	Trpc4	3	No visible phenotype.	Order From EMMA
B6;129P2-Trpc6<tm1Dg en>/H	Trpc6	9	No visible phenotype.	Order From EMMA
C3H101H-Tsk2/H	Tsk2	1	Heterozygotes can be recognised at 1 to 2 weeks of age by a tightness of the skin across the shoulders when picked up. The mice are fully viable and fertile.	Order From EMMA
Tyr<c-37Hch>	Tyr<c-37Hch>	UN	(hair - colour, eye - colour) chinchilla	Order
Tyr<c-38Hch	Tyr<c-38Hch>	UN	(hair - colour, eye - colour) chinchilla	Order
C3H101H-Tyr<c-40H>/H	a	2	(hair - colour, eye - colour, behaviour - sight) albino	Order
C3H101H-Tyr<c-40H>/H	Tyr<c-40H	UN	(hair - colour, eye - colour, behaviour - sight) albino	Order
Tyr<c-42H>	Tyr<c-ch>	7	(hair - colour, eye - colour, behaviour - sight) albino.	Order
Tyr<c-42H>	Tyr<c-42H>	UN	(hair - colour, eye - colour, behaviour - sight) albino.	Order
Tyr<c-43H>	Tyr<c-ch>	7	(hair - colour, eye - colour, behaviour - sight) albino	Order
Tyr<c-43H>	Tyr<c-43H>	UN	(hair - colour, eye - colour, behaviour - sight) albino	Order
C3H101H-Tyr<c-44H>	Tyr<c-44H>	7	(hair - colour, eye - colour, behaviour - sight) albino	Order
C3H101H-Tyr<c-45H>	Tyr<c-45H>	7	(hair - colour, eye - colour, behaviour - sight) albino	Order
C3H101H-Tyr<c-46H>	Tyr<c-46H>	7	(hair - colour, eye - colour, behaviour - sight) albino	Order
C3H101H-Tyr<c-47H>/H	Tyr<c-47H>	UN	(hair - colour, eye - colour, behaviour - sight) albino	Order
Tyr<c-49Hch>	Tyr<c-49Hch>	UN	(hair - colour, eye - colour, behaviour - sight) albino	Order
Tyr<c-50H>	Tyr<c-50H>	UN	(hair - colour, eye - colour, behaviour - sight) albino	Order
Tyr<c-51H>	Tyr<c-51H>	UN	(hair - colour, eye - colour, behaviour - sight) albino	Order
Tyr<c-54Hch>	Tyr<c-54Hch>	UN	(hair - colour, eye - colour) chinchilla	Order
Tyr<c-55H>	Tyr<c-ch>	7	(hair - colour, eye - colour, behaviour - sight) albino	Order
Tyr<c-55H>	Tyr<c-55H>	UN	(hair - colour, eye - colour, behaviour - sight) albino	Order
C3H101H-Tyr<c-em>/H	Tyr<c-em>	7	(hair - colour, eye - colour) chinchilla extreme mottled. Extreme dilution of coat.	Order From EMMA
C3H101H-Tyr<c-m>/H	Tyr<c-m>	7	(hair - colour, eye - colour) chinchilla mottled	Order
C3H101H-Tyr<c-r>/H	Tyr<c-r>	7	(hair - colour, eye - colour) ruby-eyed	Order
C3H101H-Tyrp1<b-55H> /H	Tyrp1<b-55H>	UN	(hair - colour) brown.	Order
C3H101H-Tyrp1<b-65H> /H	Tyrp1<b-65H>	UN	(hair - colour) brown	Order
C58-Tyrp1<B-lt>/H	Tyrp1<B-lt>	4	(hair - colour) heterozygotes have light underfur, homozygotes almost white hair except tips	Order
C3H101H-Ufde/H			Affected individuals have one or both ears low set and reduced in size.	Order
C3H101H-Lnp<Ul>/H	Lnp<Ul>	2	Ulnaless.	Order
UMLC-TM/12			Statistically lowered body weight & plasma levels of glucose after an overnight fast at 12 & 16 wks of age. DEXA at 14 wks: decreased body weight, lean & total tissue, BMD & BMC.	Order
UMLC-TM/6			Statistically elevated body weight & plasma levels of glucose, leptin & adiponeptin after an overnight fast at 12 & 16 wks of age. In addition elevated levels of insulin at 16wks of age. DEXA at 14wks: increased fat mass & % fat.	Order
C57BL/6Apb-Card11<un m>/Apb	Card11<unm>	5	The mice make poor antibody responses, and as they age they develop atopic dermatitis and hyper-IgE, with red itchy ears & weepy eyes, progressing to badly eroded skin from itching.	Order From EMMA
UTR/mdx (TEX)			This stock contains a tetracyclin inducible utrophin transgene when crossed with MCK-tTA mice.	Order From EMMA
Utrn<+/->	Utrn<+/->	UN	Abnormal neuromuscular junction morhpology.	Order
Utrn<-/->	Utrn<-/->	UN	Abnormal neuromuscular junction morhpology	Order
v<ALB>	Cdh23<v-Alb>	10	Waltzer Albany.	Order From EMMA
C3H;C-Vng/H	Vng	5	Small. One low ear.	Order From EMMA
VANIMMA			Under investigation: not severely immunocompromised.	Order
B6.129P2-Vnn1<tm1Pna >/H	Vnn1<tm1Pna>	10		Order
B6.129P2-Vnn1<tm1Pna >/H	Vnn1<tm1Pna>	10		Order
VAV-NPM/ALK			Mice develop lymphoid tumours from 6 months of age.	Order From EMMA
B6;129P2-Vipr1<tm1Dg en>/H	Vipr1	9	No visible phenotype	Order From EMMA
C3H101H-Vm/H			Heterozygote males have a high probability of being sterile. Visceral myopathy. Off white coat colour, intestinal problems in some animals. Males may be sterile. Older animals develop tremors. Homozygotes die soon after birth with major kidney abnormalities.	Order
VM/Dk				Order
STOCK Kit<W>/H	Kit<W>	5	Dominant white spotting	Order
B6129-Tg(Wap-cre)117 38Mam	Tg(Wap-cre)11738Mam	UN	There is no abnormal phenotype. Albino, black or white bellied Agouti.	Order
Ward Wines 5			Small increase in kidney size, possible late-onset cyst formation.	Order
C3H;C-Egfr<Wa5>/H	Egfr<Wa5>	11	Small eyes, eyes open at birth, curly whiskers and coat. Heterozygotes have open eyelids and curly whiskers at birth. The first coat has a crimped appearance and subsequent coats are wavy/rough.	Order From EMMA
wavy coat			Mice carrying this mutation have a wavy coat.	Order From EMMA
C3H;C-Whto/H	Whto	7	White toes. Heterozygous Whto mice display white belly spots and/or white toes. Homozygotes would appear to be embryonic lethal.	Order From EMMA
STOCK Whrn<wi>/H	Whrn<wi>	4	Deaf, head tossing and circling. Whirler.	Order From EMMA
Wnt2b			No visible phenotype	Order
C3H101H-Wnt3a<vt>/H	Wnt3a<vt>	11	(1) vestigial tail (2) Homozygotes have very short tails, varying form complete absence to about half normal length.	Order
STOCK Wnt3a<vt>Foxq1 <sa>Muted<mu>/H	Muted<mu>	13	Vestigial tail.	Order
	Wnt3a<vt>	11
	Foxq1<sa>	13
C3H101H-Eef1a2<wst>/ H	Eef1a2<wst>	2	Wasted homozygotes can be recognised at 20 days of age by tremor and uncoordinated body movements. They develop progressive paralysis and do not survive beyond 30 days. The wasted heterozygotes have normal viability. Also contains Ra. The ragged heterozygotes have thin, ragged coats. The homozygotes are almost naked and are semi-lethal.	Order
C3H101H-Xic<a>	Xic<a>	X		Order
Xce<a> Pgk1<a>	Pgk1<a>	UN		Order
Xce<a> Pgk1<a>	Xce<a>	UN		Order
Xce<b> Atp7a<Mo-blo>	Xce<b>	UN		Order
Xce<b> Atp7a<Mo-blo>	Atp7a<Mo-blo>	UN		Order
Xce<b> Pgk1<a>	Xce<b>	UN		Order
Xce<b> Pgk1<a>	Pgk1<a>	UN		Order
Xce<b>, Ta<Fa>	Xce<b>	UN		Order
Xce<c> Pgk1<b>	Xce<c>	UN		Order
Xce<c> Pgk1<b>	Pgk1<b>	UN		Order
Xla			Anaemia in females, seen at birth to 2 days old and may be small.	Order From EMMA
XO	Eda<Ta>	X		Order
XO	Atp7a<Mo-blo>	X		Order
C3H101H-Xs/H	Xs	7	Extra-toes spotting	Order From EMMA
Y<d-1>				Order
Y<d-2>				Order
Y<d-3>				Order
Y<d-5>				Order
Y<d-6>				Order
Y<d4>				Order
Y<dr1>				Order
Y<dr2>				Order
Y<dr3>				Order
Y<dr4>				Order
Y<dr5>				Order
C57BL/6J-Chr Y<POS>/ H			May show XY sex reversal and hermaphroditism.	Order
C3H;C-Ankrd11<Yod>/H	Ankrd11<Yod>	8	Craniofacial, broad face. Heterozygotes (Ankrd11<Yod>/+) have readily distinguishable craniofacial features. Further to this, abnormal bone morphology including an abnormally small growth plate, negligible chondrocyte hypertrophy and a dramatically reduced zone of woven bone formation have been detected.	Order
C3H.Cg-Ankrd11<Yod>/ H	Ankrd11<Yod>	8	Craniofacial, broad face. Heterozygotes (Ankrd11<Yod>/+) have readily distinguishable craniofacial features. Further to this, abnormal bone morphology including an abnormally small growth plate, negligible chondrocyte hypertrophy and a dramatically reduced zone of woven bone formation have been detected.	Order From EMMA
YZ15			Investigating how expression of Igf2 and H19 are regulated is of relevance to understanding Beckwith Weidemann syndrome. The physiological impact of over expressing H19 is not fully characterised. Unlike low copy number lines, the Igf2 LacZ gene does not show appropriate reciprocal imprinting in YZ15 mice as it is expressed from both parental alleles.	Order From EMMA
YZ17			Investigating how expression of Igf2 and H19 are regulated is of relevance to understanding Beckwith Weidemann syndrome. The physiological impact of over expressing H19 is not fully characterised. Deletion of the intergenic region with Cre recombinase results in partial (mesoderm specific) reactivation of Igf2 LacZ expression following maternal transmission.	Order From EMMA
YZ20			Investigating how expression of Igf2 and H19 are regulated is of relevance to understanding Beckwith Weidemann syndrome. The physiological impact of over?expressing H19 is not fully characterised.	Order From EMMA
YZ46			Investigating how expression of Igf2 and H19 are regulated is of relevance to understanding Beckwith Weidemann syndrome. The physiological impact of over expressing H19 is not fully characterised.	Order From EMMA
YZ8			Investigating how expression of Igf2 and H19 are regulated is of relevance to understanding Beckwith Weidemann syndrome. The physiological impact of over expressing H19 is not fully characterised. The imprinted H19 gene is only expressed when transmitted through the maternal germline. After paternal transmission the gene is repressed. The Igf2 LacZ gene shows appropriate reciprocal imprinted behaviour (paternal allele specific expression, maternal repression).	Order From EMMA
ZA1	a<e>	2		Order
	Tyrp1<b>	4
	Tyr<c-ch>	7
	Dock7<m>	4
C3H101H-a<t>Tyrp1<b- cH>Tyr<c-ch>/H	a<t>	2		Order
	Tyr<c-ch>	7
	Tyrp1<b-cH>	4

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