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KitWads
Chemically induced Allele Detail
Summary
Symbol: KitWads
Name: KIT proto-oncogene receptor tyrosine kinase; white anemic deaf sterile
MGI ID: MGI:3573757
Synonyms: Wadsm
Gene: Kit  Location: Chr5:75735647-75817382 bp, + strand  Genetic Position: Chr5, 39.55 cM
Alliance: KitWads page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThe mutation was shown by sequence analysis to be a T-to-C transition missense mutation at nucleotide 2567, resulting in a phenylalanine to serine substitution at amino acid 856 of the encoded protein. This conserved residue is located in the second protein tyrosine kinase domain. (J:96391)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 13 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:96391 Ruan HB, et al., Identification of a Novel Point Mutation of Mouse Proto-Oncogene c-kit Through N-Ethyl-N-nitrosourea Mutagenesis. Genetics. 2005 Feb;169(2):819-31
All:  5 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