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Shsm
Radiation induced Allele Detail
Summary
Symbol: Shsm
Name: shaker small
MGI ID: MGI:5320604
Gene: Shsm  Location: unknown  Genetic Position: Chr4, Syntenic
Alliance: Shsm page
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Radiation induced
Inheritance:    Dominant
Phenotypes
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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 Shsm Mutation:  0 strains or lines available
Notes
Linkage test with Tyrp1 placed Shsm 36.1 cM +/- 4.2 cM away. There was no evidence of linkage to the distal marker Espn< je>, therefore Shsm is likely to lie proximal to Tyrp1 and thus close to the centromere.
References
Original:  J:90559 The Mammalian Genetics Unit at Harwell, Information obtained from the Mammalian Genetics Unit, Medical Research Council (MRC), Harwell, UK. Unpublished. 2004-2013;
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