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Allele : Adam17<woe> a disintegrin and metallopeptidase domain 17; waved with open eyelids

Primary Identifier  MGI:3625359 Allele Type  Spontaneous
Gene  Adam17 Inheritance Mode  Recessive
Strain of Origin  C57BL/6 Is Recombinase  false
Is Wild Type  false
molecularNote  A spontaneous C to T transition at coding nucleotide 794 (c.794C>T) in exon 7 results in the amino acid substitution of threonine with methionine at position 265 (p.T265M). This mutation also disrupts splicing. The major transcript lacks exon 7, which corresponds to residues 252-281 of the metalloprotease domain. The absence of mature protein expression was confirmed by western blot analysis on mouse embryonic fibroblast extracts. The truncated product is functionally inactive but exhibits constitutive and stimulated substrate shedding.
  • mutations:
  • Single point mutation
  • synonyms:
  • Adam17<T265M>,
  • Adam17<delta252-281>,
  • Adam17<T265M>,
  • Adam17<deltaexon7>,
  • Adam17<delta252-281>,
  • Adam17<deltaexon7>,
  • wa3,
  • wa3
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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

6 Publication categories