KitW-vkd
Spontaneous Allele Detail
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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
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Alliance: |
KitW-vkd page
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Allele Type: |
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Spontaneous |
Mutation: |
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Single point mutation
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Mutation details: The 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)
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View phenotypes and curated references for all genotypes (concatenated display).
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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
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Carrying any Kit Mutation: |
182 strains or lines available
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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) |
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