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KitWhc1
Chemically induced Allele Detail
Summary
Symbol: KitWhc1
Name: KIT proto-oncogene receptor tyrosine kinase; white coat
MGI ID: MGI:3760742
Gene: Kit  Location: Chr5:75735647-75817382 bp, + strand  Genetic Position: Chr5, 39.55 cM
Alliance: KitWhc1 page
Germ cell phenotypes of KitMhdasco1/KitMhdasco1, KitMhdasow3/KitMhdasow3, KitMhdasco5/KitMhdasco5, Kittm1Alf/KitMhdasow3 and KitWhc1/KitWhc1 mice

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C3Fe;B6
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsAn A to T transversion results in an F809L amino acid residue substitution. This mutation was found in a mutagenesis screen carried out at Orleans. (J:125831)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Kit Mutation:  182 strains or lines available
References
Original:  J:125831 Magnol L, et al., KIT is required for hepatic function during mouse post-natal development. BMC Dev Biol. 2007;7:81
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
10/29/2024
MGI 6.24
The Jackson Laboratory