About   Help   FAQ
Mc1rmpc59H
Spontaneous Allele Detail
Summary
Symbol: Mc1rmpc59H
Name: melanocortin 1 receptor; muta-ped-c3pde 59, Harwell
MGI ID: MGI:5791971
Gene: Mc1r  Location: Chr8:124133846-124137483 bp, + strand  Genetic Position: Chr8, 72.1 cM
Alliance: Mc1rmpc59H page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Harwell ENU Mutagenesis
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Insertion
    Spontaneous insertion of an intracisternal A-particle. (J:234901)
Inheritance:    Recessive
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Mc1r Mutation:  43 strains or lines available
References
Original:  J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory