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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
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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:  182 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)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory