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EXPH5, exophilin 5

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  • Gene Overview
  • Interaction Network
  • Sequence Verification

EXPH5, exophilin 5

  • The protein encoded by this gene is a member of the synaptotagmin-like protein (Slp) family lacking a C2 domain. It contains an N-terminal synaptotagmin-like homology domain (SHD), and is a ras-related protein Rab-27B effector protein. This protein is thought to be involved in exosome secretion and intracellular vesicle trafficking. Reduced expression of this gene results in keratin filament defects. Mutations in this gene have been associated with some cases of epidermolysis bullosa, an inherited skin fragility disorder. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]

  • Gene Synonyms (SLAC2-B, SLAC2B, exophilin-5, slp homolog lacking C2 domains b, synaptotagmin-like homologue lacking C2 domains b, synaptotagmin-like protein homolog lacking C2 domains b,)
  • NCBI Gene ID: 23086
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>B4E1U8
    UNIPROT ID#>>Q6AI59
    UNIPROT ID#>>B4E2C3
    UNIPROT ID#>>Q8NEV8
    UNIPROT ID#>>Q149M6
  • 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.

exophilin 5 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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