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Allele : Wdfy3<disc> WD repeat and FYVE domain containing 3; disconnected

Primary Identifier  MGI:5795594 Allele Type  Chemically induced (ENU)
Attribute String  Hypomorph Gene  Wdfy3
Strain of Origin  C57BL/6J Is Recombinase  false
Is Wild Type  false
molecularNote  This mutation was identified in a forward genetics screen for mutations affecting forebrain development in mice. A single nonsense mutation in exon 59 of 67 of the Wdfy3 gene (T to A at position 9,683 of NM_172882, aa 3,046 of 3,508) was identified as the causative mutation, and introduces a premature stop codon.
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

3 Publication categories