Title Phenotype Contact
STOCK Whrn<wi>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1857090 Whrn<wi> MGI:2682003 Whrn
Deaf, head tossing and circling. Whirler. Contact
STOCK Xpo4<Gt(PT1-ATG)3EVal>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5490885 Xpo4<Gt(PT1-ATG)3EVal> MGI:1888526 Xpo4
Phenotypically normal. Contact
STOCK Yod1<tm1aNarl>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2442596 Yod1
To see phenotype data (when available) visit www.mousephenotype.org Heterozygotes: males lose hair at 4 weeks of age, stated tat "recovery accompanies age". Contact
STOCK-Rala<tm1.2Cjm>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5505279 Rala<tm1.2Cjm> MGI:1927243 Rala
Both floxed heterozygotes and homozygotes are healthy, fertile and have a normal life span. Contact
STOCK-Ralb<tm1.2Cjm>/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5505280 Ralb<tm1.2Cjm> MGI:1927244 Ralb
Both heterozygotes and homozygotes are fertile and have a normal life span. Contact
STOCK-Tecta<tm4.1Gpr>
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5527095 Tecta<tm4.1Gpr> MGI:109575 Tecta
In Tecta<tm4.1Gpr>/<tm4.1Gpr> homozygotes the tectorial membrane is completely detached from the spiral limbus and is associated instead with the Reissner membrane. Tecta is readily detectable by immunofluorescence in the detached tectorial membrane. Heterozygotes: inner ear phenotype shows malformation of the tectorial membrane, ABR thresholds elevated by ~30 dB and an enhanced susceptibility to audiogenic seizure at low sound pressure levels. See PubMed 24363064 Legan et al Human Mol Genet 2013: Three deaf mice. Contact
STOCK-Tg(MMTV-VEGFB*)1Sjh/SjhH
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5660292 Tg(MMTV-VEGFB*)1Sjh MGI:5660296 Tg(MMTV-VEGFB*)1Sjh
The offspring of hemizygous mothers, but not hemizygous fathers, die shortly after birth. The female transgenic mice have fewer blood vessels, less blood in the mammary tissue, and impaired alveolar coverage of the fat pad, and do not produce sufficient milk for nourishment of their pups. Contact
Tardbp LCDmut (M323K)
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2387629 Tardbp
Mice carry a point mutation in a gene call Tardbp (TDP43) involved in motor neurone disease and fronto-temporal dementia. Contact
Tardbp LCDmut (M323K)
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2387629 Tardbp
Mice carry a point mutation in a gene call Tardbp (TDP43) involved in motor neurone disease and fronto-temporal dementia. Contact
Tardbp LCDmut(M323K)
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2387629 Tardbp
Mice carry a point mutation in a gene call Tardbp (TDP43) involved in motor neurone disease and fronto-temporal dementia. Contact
Tardbp RRM2mut (F210I)
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2387629 Tardbp
Tardbp<Rgsc2268> mice carry a point mutation in a gene call Tardbp (TDP43) involved in motor neurone disease and fronto-temporal dementia. Contact
Tardbp RRM2mut (F210I)
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2387629 Tardbp
Tardbp<Rgsc2268> mice carry a point mutation in a gene call Tardbp (TDP43) involved in motor neurone disease and fronto-temporal dementia. Contact
Tardbp RRM2mut (F210I)
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2387629 Tardbp
Tardbp<Rgsc2268> mice carry a point mutation in a gene call Tardbp (TDP43) involved in motor neurone disease and fronto-temporal dementia. Contact
TAS6
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5646497 Tas6 MGI:5646398 Tas6
Belly spot, white feet, head spot Contact
TBL1XR1-Y446C-EM1-B6
Allele MGI ID Allele Name Gene MGI ID Gene Name
              MGI:2441730 Tbl1xr1
Contact
Tbx22<tm1Sta>
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:4361266 Tbx22<tm1Sta>              
Heterozygotes: Males: submucous cleft palate due to reduced palatal bone formation and also display variable ankyloglossia and occasional choanal atresia. Females: normal. Homozygotes: submucous cleft palate due to reduced palatal bone formation and also display variable ankyloglossia and occasional choanal atresia. Contact
TFH/H
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:1856184 T MGI:98472 T
MGI:1857070 Itpr3<tf> MGI:96624 Itpr3
Shorter tail, blunt. Contact
Tg(ACTA2-TFPI/CD4/SELP)#aAdor
Allele MGI ID Allele Name Gene MGI ID Gene Name
MGI:5578126 Tg(ACTA2-TFPI/CD4/SELP)#aAdor MGI:5578154 Tg(ACTA2-TFPI/CD4/SELP)#aAdor
Mice express membrane tethered human TFPI-CD4 fusion protein on all alpha-SMA+ (alpha smooth muscle actin) cells. In cells with secretory granules, these will be internalised at resting state by virtue of P-selectin cytoplasmic sequence. The hTFPI (human tissue factor pathway inhibitor)inhibits tissue factor and FXa (factor Xa). Contact
Tg(OvPrP)EF50 Overexpression of transgenic ovine PrPC in brain and other tissues of this mouse line in order to confer increased susceptibility to TSE diseases compared to wild-type mice. Contact
Tg(OvPrP)EM16 A ~12 kb transgene, comprised of chimaeric DNA sequence encoding a sheep PrP (AHQ allele) coding region and mouse PrP gene promoter and 3' UTR, was used to microinject pronuclear stage FVB/N fertilised oocytes. Contact

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