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Hrm1Enu
Chemically induced Allele Detail
Summary
Symbol: Hrm1Enu
Name: lysine demethylase and nuclear receptor corepressor; mutation 1, Chang-Woo Song
MGI ID: MGI:3624265
Gene: Hr  Location: Chr14:70789652-70810988 bp, + strand  Genetic Position: Chr14, 36.32 cM
Alliance: Hrm1Enu page
Mutation
origin
Strain of Origin:  BALB/cJ
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsA G to T transition at nucleotide 3572 caused a glycine to tryptophan substitution in the repression domain 3. (J:108173)
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:108173 Nam Y, et al., A novel missense mutation in the mouse hairless gene causes irreversible hair loss: genetic and molecular analyses of Hr m1Enu. Genomics. 2006 Apr;87(4):520-6
All:  1 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