About   Help   FAQ
KitW-ei
Spontaneous Allele Detail
Summary
Symbol: KitW-ei
Name: KIT proto-oncogene receptor tyrosine kinase; Eiche's dominant spotting
MGI ID: MGI:1856510
Gene: Kit  Location: Chr5:75735647-75817382 bp, + strand  Genetic Position: Chr5, 39.55 cM
Alliance: KitW-ei page
Mutation
origin
Strain of Origin:  C57BL
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsThis allele was first defined by a noncomplementation test. There is a G-to-C substitution at coding nucleotide 1790 (transcript NM_021099) which results in the glycine at amino acid position 597 being replaced by alanine (p.G597A). (J:19931, J:28100)
Inheritance:    Semidominant
Phenotypes
Loading...
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:28100 Eiche A, et al., Dominant or recessive? Different models of expression of a spontaneous new mutation in the mouse. Hereditas. 1982;97:316-7 (Abstr)
All:  3 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory