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Allele : Smad4<E6sad> SMAD family member 4; Exon 6 splice acceptor deletion

Primary Identifier  MGI:2449701 Allele Type  Spontaneous
Gene  Smad4 Inheritance Mode  Dominant
Strain of Origin  129P2/OlaHsd Is Recombinase  false
Is Wild Type  false
molecularNote  Sequence analysis identified a deletion of a single A in the exon 6 splice acceptor site. The resultant activation of a cryptic splice site 4 nt downstream of exon 6 lead to a frameshift mutation at amino acid 261 which in turn created a nonsense mutation 71 codons downstream. RT-PCR analysis indicated decreased transcript stability, putatively due to nonsense mediated decay. Protein was undetected by Western blot analysis of homozygous mutant ES cells.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Sad,
  • Sad,
  • Smad4<E6sad>,
  • Smad4<E6sad>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

Trail: Allele

0 Driven By

6 Publication categories

Trail: Allele