Title Phenotype Contact
B6;129P2-Pde8a<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3699271 Pde8a<tm1Dgen> MGI:1277116 Pde8a
No visible phenotype. Contact
B6;129P2-Prep<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5427690 Prep<tm1Dgen> MGI:1270863 Prep
None Contact
B6;129P2-Rgs5<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3604464 Rgs5<tm1Dgen> MGI:1098434 Rgs5
No visible phenotype. Contact
B6;129P2-Scube3<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4939493 Scube3<tm1Dgen> MGI:3045253 Scube3
No visible phenotype. Contact
B6;129P2-Slc7a10<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3716074 Slc7a10<tm1Dgen> MGI:1858261 Slc7a10
No visible phenotype. Contact
B6;129P2-Sox9<tm1Gsr>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2385468 Sox9<tm1Gsr> MGI:98371 Sox9
Heterozygous and homozygous Sox9-flox mice are viable, fertile and appear normal. They can be used to conditionally inactivate Sox9 by crossing with cre recombinase-expressing mice. Contact
B6;129P2-Sycn<tm1Rja>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3046204 Sycn<tm1Rja> MGI:1915666 Sycn
Pancreatic secretion compromised. Contact
B6;129P2-Tmem67<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5292220 Tmem67<tm1Dgen> MGI:1923928 Tmem67
No visible phenotype. Contact
B6;129P2-Tpcn1<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5427695 Tpcn1<tm1Dgen> MGI:2182472 Tpcn1
No visible phenotype. Contact
B6;129P2-Tpcn1<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5427695 Tpcn1<tm1Dgen> MGI:2182472 Tpcn1
No visible phenotype. Contact
B6;129P2-Trpc4<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5427696 Trpc4<tm1Dgen> MGI:109525 Trpc4
No visible phenotype. Contact
B6;129P2-Trpc6<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5427697 Trpc6<tm1Dgen> MGI:109523 Trpc6
No visible phenotype. Contact
B6;129P2-Vipr1<tm1Dgen>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5427698 Vipr1<tm1Dgen> MGI:109272 Vipr1
No visible phenotype. Contact
B6;129S-Flrt3<tm1Rob>/RobH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3797077 Flrt3<tm1Rob> MGI:1918686 Flrt3
Mouse embryos deficient in Flrt3 display defects in headfold fusion, definitive endoderm migration and a failure of the lateral edges of the ventral body wall to fuse, leading to cardia bifida. A small proportion of homozygous mutants survive gestation and develop as viable fertile animals (<3%). Heterozygous mice have no overt phenotype. Contact
B6;129S4-Rhog<tm1Tnr>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3029009 Rhog<tm1Tnr> MGI:1928370 Rhog
Mild hyper reactivity of lymphocytes to antigen receptor engagement. Contact
B6;129S6-Rr4<tm1Hgc>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4421037 Rr4<tm1Hgc> MGI:4421017 Rr4
To date this mouse strain does not have an overt phenotype. Contact
B6;129X1-Ajuba<tm1Gdl>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3578221 Ajuba<tm1Gdl> MGI:1341886 Ajuba
Phenotype not fully analysed in vivo. Western blot analysis showed absence of ajuba LIM protein in MEFs. Contact
B6;CBA-Tg(SMN1*E134K)1Tlbt/H None. Contact
B6;CBACa-Tg(ADCYAP1R1)1Sshe/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5645747 Tg(ADCYAP1R1)1Sshe MGI:5645743 Tg(ADCYAP1R1)1Sshe
This line is a high expresser (Tg1 in publication PMID: 16823490) and causes a striking hydrocephalus related phenotype. Both homozygotes and heterozygotes: high rate of early postnatal death and dose dependent hydrocephalus and/or schizophrenia like neuropathy. Contact
B6;CBACa-Tg(ADCYAP1R1)2Sshe/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5645748 Tg(ADCYAP1R1)2Sshe MGI:5645744 Tg(ADCYAP1R1)2Sshe
This line is described as being a "medium level" expressor (Tg2 in PMID:16823490). Both homozygotes and heterozygotes: high rate of early postnatal death and dose dependent hydrocephalus and/or schizophrenia like neuropathy. Contact

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