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NPC2, NPC intracellular cholesterol transporter 2

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NPC2, NPC intracellular cholesterol transporter 2

  • This gene encodes a protein containing a lipid recognition domain. The encoded protein may function in regulating the transport of cholesterol through the late endosomal/lysosomal system. Mutations in this gene have been associated with Niemann-Pick disease, type C2 and frontal lobe atrophy. [provided by RefSeq, Jul 2008]

  • Gene Synonyms (EDDM1, HE1, NPC intracellular cholesterol transporter 2, Niemann-Pick disease type C2 protein, epididymal protein 1, epididymis secretory sperm binding protein, human epididymis-specific protein 1, tissue-specific secretory protein,)
  • NCBI Gene ID: 10577
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>P61916
    UNIPROT ID#>>A0A024R6C0
  • 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.

NPC intracellular cholesterol 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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