About   Help   FAQ
Mc1rE-so
Spontaneous Allele Detail
Nomenclature
Symbol: Mc1rE-so
Name: melanocortin 1 receptor; sombre
MGI ID: MGI:1856029
Synonyms: Eso, So
Gene: Mc1r  Location: Chr8:123407107-123410744 bp, + strand  Genetic Position: Chr8, 72.1 cM
Mutation
origin
Strain of Origin:  C3H
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA T-to-C mutation in codon 96 is predicted to result in a leucine to proline alteration at this position. (J:4636)
Inheritance:    Semidominant
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 4 strains available      Cell Lines: 0 lines available
Carrying any Mc1r Mutation:  26 strains or lines available
References
Original:  J:13077 Bateman N, Sombre, a viable dominant mutant in the house mouse. J Hered. 1961;52:186-189
All:  6 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 & Copyright Notice
Send questions and comments to User Support.
last database update
01/14/2020
MGI 6.14
The Jackson Laboratory