FVB(129P2)-Pde6b<+> Gtf2i<em2Jdd> Gtf2ird1<em2Jdd> Tyr<c-ch>/Mmjax Strain Detail MGI Mouse MGI:6429893

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FVB(129P2)-Pde6b⁺ Gtf2i^em2Jdd Gtf2ird1^em2Jdd Tyr^c-ch/Mmjax Strain Detail

Summary

Strain Name

FVB(129P2)-Pde6b⁺ Gtf2i^em2Jdd Gtf2ird1^em2Jdd Tyr^c-ch/Mmjax
Attributes

endonuclease-mediated mutation, mutant strain, spontaneous mutation
MGI ID

MGI:6429893

Other IDs

JAX:034245, MMRRC:066710-JAX

4 associated mutations

Mutation Carried	Marker
Gtf2i^em2Jdd	Gtf2i
Gtf2ird1^em2Jdd	Gtf2ird1
Pde6b⁺	Pde6b
Tyr^c-ch	Tyr

1 associated strain record at IMSR

IMSR	Repository	IMSR Strain	Why Matched
MMRRC:066710-JAX	MMRRC	FVB(129P2)-Pde6b⁺ Gtf2i^em2Jdd Gtf2ird1^em2Jdd Tyr^c-ch/Mmjax	exact match to ID

Earliest

J:284943 Kopp N, et al., Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models. Hum Mol Genet. 2019 Oct 15;28(20):3443-3465
All

2

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