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Allele : Hr<rh-Chr> lysine demethylase and nuclear receptor corepressor; rhino Christiano

Primary Identifier	MGI:3630275	Allele Type	Spontaneous
Gene	Hr	Strain of Origin	wild
Is Recombinase	false	Is Wild Type	false

molecularNote

A C-to-T transition mutation at codon 467 results in an arginine to stop codon alteration (p.R467*) in the encoded protein.

mutations:
Single point mutation

earliestPublication:
Ahmad W, et al. (1998) Molecular basis of a novel rhino (hr(rhChr)) phenotype: a nonsense mutation in the mouse hairless gene. Exp Dermatol 7(5):298-301

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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