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KitW-n
Spontaneous Allele Detail
Summary
Symbol: KitW-n
Name: KIT proto-oncogene receptor tyrosine kinase; Nagoya dominant spotting
MGI ID: MGI:1856512
Gene: Kit  Location: Chr5:75735647-75817382 bp, + strand  Genetic Position: Chr5, 39.55 cM
Alliance: KitW-n page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsAnalysis of cDNA showed this allele comprises a C-to-T transition at nucleotide 2504 (transcript NM_021099) in the tyrosine kinase domain, resulting in a change of alanine to valine at position 835 (p.A835V). Encoded c-kit protein is not expressed on the cell surface. (J:27513)
Inheritance:    Semidominant
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 Kit Mutation:  179 strains or lines available
References
Original:  J:12107 Go S, et al., Effect of W and Wv alleles on production of tissue mast cells in mice. J Hered. 1980;71(1):41-44
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
04/16/2024
MGI 6.23
The Jackson Laboratory