Title Phenotype Contact
129P2/OlaHsd-Wt1<tm1Mlh>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3794650 Wt1<tm1Mlh> MGI:98968 Wt1
Heterozygous mutant mice develop glomerulosclerosis (typical of Denys Drash Syndrome) with age. Contact
129P2/OlaHsdH-Prnp<tm2Edin>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2387688 Prnp<tm2Edin> MGI:97769 Prnp
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. Contact
129S(B6)-Gnas<tm2Kel>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3579575 Gnas<tm2Kel> MGI:95777 Gnas
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. Contact
129S(Cg)-Foxh1<tm1Jlw>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2179442 Foxh1<tm1Jlw> MGI:1347465 Foxh1
Homozygous lethal at day 8 of gestation. Contact
129S.129P2-Cited2<tm1Bha>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2179740 Cited2<tm1Bha> MGI:1306784 Cited2
Contact
129S/SvEv-Gt(ROSA)26Sor<tm1Coll>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5429346 Gt(ROSA)26Sor<tm1Coll> MGI:104735 Gt(ROSA)26Sor
No obvious phenotype. Contact
129S/SvEv-Klf13<tm1Coll>/CollH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4837928 Klf13<tm1Coll> MGI:1354948 Klf13
Mice show altered T, B cell & erythroblast differentiation. Contact
129S/SvEvBrd-Brd7<tm2a(EUCOMM)Wtsi>/WtsiH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4842893 Brd7<tm2a(EUCOMM)Wtsi> MGI:1349766 Brd7
View available phenotyping data on the IMPC portal Contact
129S/SvEvBrd-Brd7<tm2a(EUCOMM)Wtsi>/WtsiH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4842893 Brd7<tm2a(EUCOMM)Wtsi> MGI:1349766 Brd7
View available phenotyping data on the IMPC portal Contact
129S/SvEvBrd-Mta1<tm1a(EUCOMM)Wtsi>/WtsiH
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2150037 Mta1
View available phenotyping data on the IMPC portal Contact
129S/SvEvBrd-Mta1<tm1a(EUCOMM)Wtsi>/WtsiH
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2150037 Mta1
MGI:4842891 Mta1<tm1a(EUCOMM)Wtsi> MGI:2150037 Mta1
View available phenotyping data on the IMPC portal Contact
129S2(B6)-Meg3<Gt(pGTi)216Gos>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2177961 Meg3<Gt(pGTi)216Gos> MGI:1202886 Meg3
Imprinted dwarfism and thyroid hormone defects. This transgenic mouse line carries an insertional mutation with a dominant modified pattern of inheritance: heterozygous Gtl2 lacZ mice that inherited the transgene from the father show a proportionate dwarfism phenotype; whereas the penetrance and expressivity of the phenotype is strongly reduced in Gtl2 lacZ mice that inherited the transgene from the mother. On a mixed genetic background this pattern of inheritance was reversible upon transmission of the transgene through the germ line of the opposite sex whereas on a predominantly 129S2/SvPas genetic background the transgene passage through the female germ line modifies the transgene effect, such that the penetrance of the mutation was drastically reduced and the phenotype is no longer obvious after subsequent male germ line transmission. Expression of the transgene is neither affected by genetic background nor by parental legacy. It has been postulated that that the transgene insertion in Gtl2 lacZ mice affects an endogenous gene(s) required for fetal and postnatal growth and that this gene(s) is predominantly paternally expressed. Contact
129S2.129P2-Ccl6<tm1Roes>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5494646 Ccl6<tm1Roes> MGI:98263 Ccl6
None mentioned. Contact
129S2.Cg-Tg(KRT10-Igfr2*)KippsGfc/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5436057 Tg(KRT10-Igf2r*)KippsGfc              
Slightly reduced overall body weight, disproportionate reduction in size of alimentary canal and uterus. Contact
129S2;129P2-Gca<tm1Roes>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2450787 Gca<tm1Roes> MGI:1918521 Gca
Minimal. Contact
129S5;B6N-Kdm6a<tm2a(EUCOMM)Wtsi>/WtsiH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4441731 Kdm6a<tm2a(EUCOMM)Wtsi> MGI:1095419 Kdm6a
To see phenotype data (when available) visit www.mousephenotype.org Contact
129S6.129P2(Cg)-Fgfr3<tm1.1Aomw>/AomwH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3831364 Fgfr3<tm1.1Aomw> MGI:95524 Fgfr3
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. Contact
129S9.B6-a/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1855937 a MGI:87853 a
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). Contact
129S9/SvEvH-Evta/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3851189 Evta MGI:3851187 Evta
White coat with non-agouti specking and occasional non-agouti patches. Contact
2700049A03Rik<tm1.1Arte>
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5287574 2700049A03Rik<tm1.1Arte> MGI:1924217 2700049A03Rik
Crossing talpid3 floxed mutant mice with Cre mice leads to functional inactivation of the Talpid3 gene and hence loss of cilia. Contact

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