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Hrrh-bmh
Spontaneous Allele Detail
Summary
Symbol: Hrrh-bmh
Name: lysine demethylase and nuclear receptor corepressor; rhino-bald Mill Hill
MGI ID: MGI:3039558
Synonyms: hrrhbmh
Gene: Hr  Location: Chr14:70789652-70810988 bp, + strand  Genetic Position: Chr14, 36.32 cM
Alliance: Hrrh-bmh page
Mutation
origin
Strain of Origin:  C57BL/6JRj x CBA/JRj
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThe mutation in the bald Mill Hill mouse was determined to be a small 296 bp deletion of genomic DNA that includes part of exon 19 and the 3' UTR of the gene. The mutant allele is expressed in a similar pattern to the wild-type message. However the resulting protein is 150 rather than 130 kDa in size. (J:89321)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Hr Mutation:  87 strains or lines available
References
Original:  J:89321 Brancaz MV, et al., A new allele of the mouse hairless gene interferes with Hox/LacZ transgene regulation in hair follicle primordia. Exp Mol Pathol. 2004 Apr;76(2):173-81
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory