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Tyrp1b-c
Spontaneous Allele Detail
Summary
Symbol: Tyrp1b-c
Name: tyrosinase-related protein 1; brown cordovan
MGI ID: MGI:1855961
Synonyms: Tyrp1b-cJ
Gene: Tyrp1  Location: Chr4:80752360-80769956 bp, + strand  Genetic Position: Chr4, 37.89 cM
Alliance: Tyrp1b-c page
Mutation
origin
Strain of Origin:  (DBA/1 x C57BL/10)F1
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation detailsComplementation testing demonstrated that this mutation is an allele of the original brown (Tyrp1b) mutation. The Tyrp1b-c allele was found among (DBA/1 X C57BL/10)F1 offspring. Because DBA is homozygous for Tyrp1b, the mutation occurred on C57BL10.
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: 3 strains available      Cell Lines: 0 lines available
Carrying any Tyrp1 Mutation:  162 strains or lines available
Notes
Homozygous recessive mutant on a nonagouti/black background are chocolate brown and show altered melanin granule morphology. Semidominant mutants result in melanocyte degeneration causing reduced pigmentation and progressive hearing loss.
References
Original:  J:15167 Miller DS, et al., Cordovan, a new allele of black and brown color in the mouse. J Hered. 1955;46(6):293-96
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
04/16/2024
MGI 6.23
The Jackson Laboratory