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mrct
Spontaneous Allele Detail
Summary
Symbol: mrct
Name: modifier of Rinshoken cataract
MGI ID: MGI:2387332
Gene: mrct  Location: unknown  Genetic Position: Chr5, Syntenic
Alliance: mrct page
Mutation
origin
Strain of Origin:  SJL/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
    A modifier locus of the rct gene that was identified in mapping studies.
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: 0 strains available      Cell Lines: 0 lines available
Carrying any mrct Mutation:  0 strains or lines available
References
Original:  J:68340 Maeda YY, et al., Two interactive genes responsible for a new inherited cataract (RCT) in the mouse. Mamm Genome. 2001 Apr;12(4):278-83
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
04/23/2024
MGI 6.23
The Jackson Laboratory