Title Phenotype Contact
STOCK 129-Rab27b<tm1.2Seab>/SeabH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3706986 Rab27b<tm1.2Seab> MGI:1931295 Rab27b
Mice exhibit significant haemorrhagic disease - platelets demonstrated impaired aggregation with collagen and U46619 and reduced secretion of dense granules. The number of dense granules per platelet serotonin content are also reduced. Mice are fertile, have normal life span, seems to be healthy, phenotypically look normal. Contact
STOCK anan/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5568076 anan MGI:5568074 anan
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. Contact
STOCK anaya/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5568096 anaya MGI:5568094 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. Contact
STOCK andra/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5568106 andra MGI:5568104 andra
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. Contact
STOCK Arap2<Gt(PT1-ATG)9Val>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5514159 Arap2<Gt(PT1-ATG)9AVal> MGI:2684416 Arap2
Normal Contact
STOCK Bhv26/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5646243 Bhv26 MGI:5646241 Bhv26
The alternation score suggest this line has a potential short term working memory deficit. Contact
STOCK bicm2
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3709881 Mir155<tm1.1Brd> MGI:2676840 Mir155
No overt phenotype reported. Contact
STOCK Bmp7<tm1Rob>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857654 Bmp7<tm1Rob> MGI:103302 Bmp7
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. Contact
STOCK Bmp7<tm2Rob>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2136986 Bmp7<tm2Rob> MGI:103302 Bmp7
Homozygous embryonic lethal. Contact
STOCK Cacna2d1<tm1Aschw>/AschwAdlpnH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4353680 Cacna2d1<tm1Aschw> MGI:88295 Cacna2d1
Mice homozygous for this mutation exhibit a smooth muscle deficiency and increased urination. Homozygous males are impotent. Cacna2d1<tm1Aschw>/Cacna2d1<tm1Aschw> mice lack gabapentin (GPB) binding sites, show decreased basal myocardial contractility and relaxation, and decreased L-type calcium currents in cardiomyocytes. Homozygous males have reduced mechanosensory responses and delayed development of neuropathic mechanical hypersensitivity following sensory nerve injury. Heterozygotes have no overt phenotype. Contact
STOCK Cdh23<v-Alb>/WtsiH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857310 Cdh23<v-Alb> MGI:1890219 Cdh23
Waltzer Albany. Contact
STOCK Col4a1<Raw>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2178446 Col4a1<Raw> MGI:88454 Col4a1
Retinal ateriolar wiring. Shiny retinal blood vessels. Contact
STOCK Col4a1<Svc>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2178448 Col4a1<Svc> MGI:88454 Col4a1
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. Contact
STOCK Dmd<mdx> Tg(Ckm-Dmd_iDp71)MCA-1Chmb/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1856328 Dmd<mdx> MGI:94909 Dmd
MGI:2148589 Utrn<tm1Ked> MGI:104631 Utrn
MGI:5140740 Tg(Ckm-Dmd_iDp71)MCA-1Chmb              
Contact
STOCK Dmd<mdx> Tg(tetO-Utrn)1Ked/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:5140309 Tg(tetO-Utrn)1Ked
MGI:1856328 Dmd<mdx> MGI:94909 Dmd
This stock contains a tetracyclin inducible utrophin transgene when crossed with MCK-tTA mice. Contact
STOCK Dnah11<iv>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1856917 Dnah11<iv> MGI:1100864 Dnah11
MGI:1855960 Tyrp1<b> MGI:98881 Tyrp1
Situs inversus viscerum. Mice show randomisation of situs (sidedness), 50% showing a reversal of their left and right hand sides. Such mice show no obvious deleterious effects. Mice with reversed viscera can be identified as soon after birth as milk has been ingested and until they are 4-5 days old. Using stomach and spleen position mice are classified neonatally for visceral inversions. Contact
STOCK Dync1h1<Loa>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2447991 Dync1h1<Loa> MGI:103147 Dync1h1
Legs at odd angle. Contact
STOCK Egr2<tm3Pch> Tg(CD2-cre)4Kio/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2183227 Egr2<tm3Pch> MGI:95296 Egr2
MGI:2449947 Tg(CD2-icre)4Kio MGI:2449946 Tg(CD2-icre)4Kio
Spontaneous autoimmune diseases start at late age (12 months). Contact
STOCK Epo<Tg(SV40T/Epo)134.3LCPjr>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3767166 Epo<Tg(SV40T/Epo)134.3LCPjr>              
Homozygotes have incomplete epo deficiency and are anaemic. Contact
STOCK Fgf7<tm1e(EUCOMM)Hmgu>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4455930 Fgf7<tm1e(EUCOMM)Hmgu> MGI:95521 Fgf7
View available phenotyping data on the IMPC portal Contact

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