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Vm
Chemically and radiation induced Allele Detail
Summary
Symbol: Vm
Name: visceral myopathy
MGI ID: MGI:5320605
Gene: Vm  Location: unknown  Genetic Position: Chr17, Syntenic
Alliance: Vm page
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Chemically and 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: 2 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 Vm Mutation:  0 strains or lines available
Notes
Male mice received triethylenemelamine, two doses of hydroxyurea and 6Gy X rays. Vm has been mapped: T - 6.5 cM+/-1.2cM - Vm - 7.6cM+/-1.7cM - tf
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 Unpublished. 2004-2013;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
11/12/2024
MGI 6.24
The Jackson Laboratory