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WIPF1, WAS/WASL interacting protein family member 1

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WIPF1, WAS/WASL interacting protein family member 1

  • This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (WAS/WASL-interacting protein family member 1, WASP-interacting protein, Wiskott-Aldrich syndrome protein interacting protein, protein PRPL-2, testicular tissue protein Li 226, PRPL-2, WAS2, WASPIP, WIP,)
  • NCBI Gene ID: 7456
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>A0A140VJZ9
    UNIPROT ID#>>O43516
    UNIPROT ID#>>Q2YDC4
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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