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SPNS2, sphingolipid transporter 2

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  • Gene Overview
  • Interaction Network
  • Sequence Verification

SPNS2, sphingolipid transporter 2

  • The protein encoded by this gene is a transporter of sphingosine 1-phosphate, a secreted lipid that is important in cardiovascular, immunological, and neural development. Defects in this gene are a cause of early onset progressive hearing loss. [provided by RefSeq, Jul 2016]

  • Gene Synonyms (DFNB115, SLC62A2, protein spinster homolog 2, SPNS sphingolipid transporter 2, spinster homolog 2,)
  • NCBI Gene ID: 124976
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q8IVW8
  • 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.

sphingolipid transporter 2 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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