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Hrrh-7J
Spontaneous Allele Detail
Summary
Symbol: Hrrh-7J
Name: lysine demethylase and nuclear receptor corepressor; rhino 7 Jackson
MGI ID: MGI:1856062
Gene: Hr  Location: Chr14:70789652-70810988 bp, + strand  Genetic Position: Chr14, 36.32 cM
Alliance: Hrrh-7J page
Mutation
origin
Strain of Origin:  C57BL/6J-Hbbp
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsThis allele was initially defined by a noncomplementation test with Hrhr and subsequently defined as a G to A transition at position 1253 of the cDNA (c.G1253A) resulting in a stop codon in place of a tryptophan in exon 3, resulting in premature termination. (J:57947)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Hr Mutation:  84 strains or lines available
References
Original:  J:30778 Sweet HO, et al., Remutations at The Jackson Laboratory (Update to Mouse Genome 1993; 91:862-5 - J16313). Mouse Genome. 1995;93(4):1030-4
All:  4 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
04/16/2024
MGI 6.23
The Jackson Laboratory