Title Phenotype Contact
LV5 transgenic
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5556056 Tg(CAG-LARGE)126Fmu MGI:5556055 Tg(CAG-LARGE)126Fmu
No overt phenotype. Contact
M1073B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5515456 M1073b MGI:5515454 M1073b
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
Embryonic lethal. Contact
M1185B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:5515459 M1185b MGI:5515457 M1185b
Embryonic lethal Contact
M1239B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:3607721 sau MGI:3607718 sau
Embryonically lethal Contact
M1616B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:5515462 M1616b MGI:5515460 M1616b
Embryonic lethal. Contact
M1645B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:5515465 M1645b MGI:5515463 M1645b
Embryonic lethal. Contact
M241B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:5515441 M241b MGI:5515439 M241b
Embryonic lethal - not fully penetrant. Forebrain truncation abnormality. Contact
M369B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:5515444 M369b MGI:5515442 M369b
Embryonic lethal Contact
M624B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:5515450 M624b MGI:5515448 M624b
Embryonic lethal Contact
M876B
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857026 Foxq1<sa> MGI:1298228 Foxq1
MGI:5515453 M876b MGI:5515451 M876b
Embryonic lethal in a Mut sa/++ (heterozygous) intercross. Line is not an embryonic lethal when crossed to the Del36H deletion. Contact
Math1-Bmi1 (Cross 2) Contact
Nbr1<D50R>
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:108498 Nbr1
Point mutation disrupts Nbr1-p62 PB1 mediated protein interaction. Phenotype of altered bone remodelling- increased osteoclast differentiation, and resulting early osteoporotic phenotype. Contact
Nephertiti No visible phenotype. Mice develop nephrotic range proteinuria at a young age and has abnormal liver histology, similar to Lafora body disease. Contact
P3h2<em1(IMPC)H>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:6257567 P3h2<em1(IMPC)H>              
Contact
PDE2A-D479G-CAS-B6N
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2446107 Pde2a
Contact
Prnp<a(108L_189V)> (DD) No phenotype Contact
Pro-Cre None. Contact
R26R-ECFP
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2449039 Gt(ROSA)26Sor<tm2(ECFP)Cos> MGI:104735 Gt(ROSA)26Sor
None visible. Have the potential to express ECFP in any tissue, upon Cre mediated activation. Contact
R26R-EYFP
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:2449038 Gt(ROSA)26Sor<tm1(EYFP)Cos>              
No reported overt phenotype in the absence of Cre expression. Contact
RIII//???
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:3045029 Prnp<a> MGI:97769 Prnp
White mouse. Susceptible to CJD/vCJD disease progression upon exposure to viable prion agents. Contact

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