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SAMSN1, SAM domain, SH3 domain and nuclear localization signals 1

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SAMSN1, SAM domain, SH3 domain and nuclear localization signals 1

  • SAMSN1 is a member of a novel gene family of putative adaptors and scaffold proteins containing SH3 and SAM (sterile alpha motif) domains (Claudio et al., 2001 [PubMed 11536050]).[supplied by OMIM, Mar 2008]

  • Gene Synonyms (SAM domain-containing protein SAMSN-1, SAM and SH3 domain containing 2, SAM domain, SH3 domain and nuclear localisation signals, 1, SAM domain, SH3 domain and nuclear localization signals protein 1, SH3-SAM adaptor protein, Src homology domain 3 (SH3)-containing adapter protein SH3 lymphocyte protein 2, hematopoietic adapter-containing SH3 and sterile I+/--motif (SAM) domains 1, hematopoietic adapter-containing SH3 and sterile alpha-motif (SAM) domains 1, hematopoietic adaptor containing SH3 and SAM domains 1, nuclear localization signals, SAM and SH3 domain containing 1, HACS1, NASH1, SASH2, SH3D6B, SLy2,)
  • NCBI Gene ID: 64092
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q9NSI8
    UNIPROT ID#>>S6FRS6
  • 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.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

SAM domain, SH3 domain and nuclear localization signals 1 interacts with:

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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