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Allele : Kit<Wads> KIT proto-oncogene receptor tyrosine kinase; white anemic deaf sterile

Primary Identifier  MGI:3573757 Allele Type  Chemically induced (ENU)
Gene  Kit Inheritance Mode  Semidominant
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  The mutation was shown by sequence analysis to be a T-to-C transition missense mutation at nucleotide 2567, resulting in a phenylalanine to serine substitution at amino acid 856 of the encoded protein. This conserved residue is located in the second protein tyrosine kinase domain.
  • mutations:
  • Single point mutation
  • synonyms:
  • Wads<m>,
  • Wads<m>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

7 Publication categories