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Allele : Sox9<Bbfc> SRY (sex determining region Y)-box 9; babyface

Primary Identifier	MGI:5546026	Allele Type	Chemically induced (ENU)
Attribute String	Hypomorph	Gene	Sox9
Inheritance Mode	Semidominant	Strain of Origin	C57BL/6J
Is Recombinase	false	Is Wild Type	false

molecularNote

A C-to-T transition mutation results in a threonine to methionine missense mutation at codon 87 (p.T87M).

mutations:
Single point mutation

earliestPublication:
Fairfield H, et al. (2015) Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders. Genome Res 25(7):948-57

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

Other

1 Carried By

0 Driven By

4 Publication categories

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