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rs
Spontaneous Allele Detail
Summary
Symbol: rs
Name: recessive spotting
MGI ID: MGI:1857022
Gene: rs  Location: Chr5:35735349-101260904 bp  Genetic Position: Chr5, Syntenic
Alliance: rs page
Mutation
origin
Strain of Origin:  C3H/HeJ
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
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 rs Mutation:  3 strains or lines available
Notes
This allele is a semidominant mutation: 21% of known heterozygous offspring also have an abnormal phenotype and incomplete penetrance due to the genetic background, which likely explains the recovery rate.
References
Original:  J:13456 Dickie MM, Recessive spotting. Mouse News Lett. 1966;35:31
All:  2 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
03/19/2024
MGI 6.23
The Jackson Laboratory