About   Help   FAQ
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
Loading...
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory