Title 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
PDE2A-D479G-CAS-B6N Contact
Prnp<a(108L_189V)> (DD) No phenotype Contact
Pro-Cre None. Contact
R26R-ECFP None visible. Have the potential to express ECFP in any tissue, upon Cre mediated activation. Contact
R26R-EYFP No reported overt phenotype in the absence of Cre expression. Contact
RIII//??? White mouse. Susceptible to CJD/vCJD disease progression upon exposure to viable prion agents. Contact
SAA2 None. Contact
Sgms1 Knockout 1 EPD0725_2_G05 To see phenotype data (when available) visit www.mousephenotype.org Contact
SJL.129(B6)-Nr1i2<tm1Sakl>/H The PXR regulates the inducible expression of the major drug metabolising cytochrome P450 3a subfamily of enzymes, which are also responsible for the metabolism of elevated levels of bile acids. Knock out animals therefore do not respond to inducers such as pregnenolone 16alpha carbonitrile and show sensitivity to elevated bile acid levels (liver damage). The SJL background shows an unusual constititively high level of portal tract inflammation (Jones DE, Palmer JM, Kirby JA, De Cruz DJ, McCaughan GW, Sedgwick JD, Yeaman SJ, Burt AD, Bassendine MF. Experimental autoimmune cholangitis: a mouse model of immune-mediated cholangiopathy. Liver. 2000 Oct;20(5):351-6.). This strain (along with its wild type) is therefore a model for examining the effects of drugs and bile acids on portal tract inflammation. Contact
SJL/J Lgals1tm1Rob These mice are susceptible to Theiler Murine Encephalomyelitis Virus infection and can be used to model primary progressive multiple sclerosis. During the backcrossing there was high mortality rate amongst litters and very poor breeding due to aversion to other mouse strain pheromones. SJL/J males also exhibited significant aggression often resulting in amyloidosis (sequel of social submissiveness and consequent wounds) in female breeding partners which were often very severe and required culling. Contact
SJL/J Lgals3tm1Poi These mice are susceptible to Theilers Murine Encephalomyelitis Virus infection and can be used to model primary progressive multiple sclerosis. During the backcrossing there was high mortality rate amongst litters and very poor breeding due to aversion to other mouse strain pheromones. SJL/J males also exhibited significant aggression often resulting in amyloidosis (sequel of social submissiveness and consequent wounds) in female breeding partners which were often severe and required culling. Contact
Slc22a6-CreERT2 Heterozygous and homozygous Slc22a6-CreERT2 mice are viable and display no discernible phenotype. Upon administration of tamoxifen recombinase activity is induced specifically in the epithelia of proximal renal tubules. Contact
SPC tetCre loxP VEGF Upon administration of doxycycline, exon 3 of Vegf is deleted from type II alveolar epithelial cells in the lung parenchyma. Contact
StarD10-tg-F10 Overexpression of the transgene when crossed with mouse expressing the reverse tetracycline transactivator and given doxycycline (possibility of a tissue specific overexpression). The transgene copy number for this line was evaluated by qPCR and estimated at 25 copies ([23.88 - 25.43], n = 14). The expression level in islets level was measured by western blot after induction by 2g/L doxycycline in drinking water and estimated to be 120% of the control expression. In vivo phenotype: The animals were crossed with RIP7-rtTA mice allowing overexpression of the transgene specifically in pancreatic beta-cells. The doxycycline was added in drinking water (2g/L) from 5 weeks of age and intra-peritoneal glucose tolerance tests (IPGTT, 1g/kg glucose) were performed at 8, 12 and 16-week-old. The resulting line had no differences with control mice on chow diet. This line has not yet been tested on HFD. Contact
StarD10-tg-F3 Overexpression/Repression of the transgene when crossed with mice expressing (reverse) tetracycline transactivator and given doxycycline. The transgene copy number for this strain was evaluated by qPCR and estimated to be 15 copies ([14.50 - 16.44], n = 4). The expression level in islets level was measured by western blot after induction by 2g/L doxycycline in drinking water and estimated to be 250 % of the control expression. In vivo phenotype: Crossing with RIP7-rtTA mice allowed overexpression of the transgene specifically in pancreatic beta-cells. The doxycycline was added in drinking water (2g/L) from 5 weeks of age and intra-peritoneal glucose tolerance tests (IPGTT, 1g/kg glucose) were performed at 8, 12 and 16-week-old. The resulting line showed no differences with control mice on chow diet. On high fat diet (65% calories from fat; from 5-week-old) the transgenic mice had a lower weight and better glucose tolerance than control at 16-week-old without significant difference in the intra-peritoneal insulin tolerance test. Contact
STOCK 129-Rab27b<tm1.2Seab>/SeabH 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 Adam11<tm1a(KOMP)Mbp>/H To see phenotype data (when available) visit www.mousephenotype.org Contact
STOCK anan/H 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 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

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