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Allele : mwfh<C3HeB/FeJLe> modifier of white forlock hypopigmentation; C3HeB/FeJLe

Primary Identifier	MGI:3617475	Allele Type	QTL
Gene	mwfh	Inheritance Mode	Recessive
Strain of Origin	C3HeB/FeJLe	Is Recombinase	false
Is Wild Type	false

description	This locus modifies the hypopigmentation phenotype of the Sox10^Dom> mutation.
molecularNote	This allele confers increased incidence of white forelock hypopigmentation compared to C57BL/6JLe.

earliestPublication:
Southard-Smith EM, et al. (1999) The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome. Genome Res 9(3):215-25

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

Other

0 Carried By

0 Driven By

3 Publication categories

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