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ERLIN2, ER lipid raft associated 2

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ERLIN2, ER lipid raft associated 2

  • This gene encodes a member of the SPFH domain-containing family of lipid raft-associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1,4,5-trisphosphate (IP3) signaling by mediating ER-associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia-18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012]

  • Gene Synonyms (erlin-2, SPFH domain family, member 2, endoplasmic reticulum lipid raft-associated protein 2, epididymis secretory sperm binding protein, spastic paraplegia 18 (autosomal dominant), stomatin-prohibitin-flotillin-HflC/K domain-containing protein 2, C8orf2, Erlin-2, NET32, SPFH2, SPG18,)
  • NCBI Gene ID: 11160
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>O94905
  • 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.

ER lipid raft associated 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.

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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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