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KitW-vkd
Spontaneous Allele Detail
Summary
Symbol: KitW-vkd
Name: KIT proto-oncogene receptor tyrosine kinase; vickid
MGI ID: MGI:3047218
Synonyms: VIable C-Kit Deficient
Gene: Kit  Location: Chr5:75735647-75817382 bp, + strand  Genetic Position: Chr5, 39.55 cM
Alliance: KitW-vkd page
Mutation
origin
Strain of Origin:  STOCK KitW
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsThe complete molecular nature of this allele has not yet been determined. Restriction site analysis and sequenceing identified the W mutation in which a G-to-A transition exists in the splice donor site of exon 10-intron 10 (changing it from G-GT to G-AT), resulting in the aberrant splicing of exon 9 to 11, skipping exon 10 which encodes the transmembrane domain. Protein produced from this allele could not be discerned from the product of the KitW allele by immunoprecipitation. (J:79128)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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:79128 Waskow C, et al., Viable c-Kit(W/W) Mutants Reveal Pivotal Role for c-Kit in the Maintenance of Lymphopoiesis. Immunity. 2002 Sep;17(3):277
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
11/12/2024
MGI 6.24
The Jackson Laboratory