NPC1

NPC1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNPC1, NPC, NPC intracellular cholesterol transporter 1, SLC65A1, POGZ
External IDsOMIM: 607623; MGI: 1097712; HomoloGene: 228; GeneCards: NPC1; OMA:NPC1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000271

NM_008720

RefSeq (protein)

NP_000262

NP_032746

Location (UCSC)Chr 18: 23.51 – 23.59 MbChr 18: 12.32 – 12.37 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
NPC1 gene is located on the long (q) arm of chromosome 18 at position 11.2.

Niemann-Pick disease, type C1 (NPC1) is a membrane protein that mediates intracellular cholesterol trafficking in mammals. In humans the protein is encoded by the NPC1 gene (chromosome location 18q11).[5][6]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000141458Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024413Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: NPC1 Niemann-Pick disease, type C1".
  6. ^ Carstea ED, Polymeropoulos MH, Parker CC, et al. (March 1993). "Linkage of Niemann-Pick disease type C to human chromosome 18". Proceedings of the National Academy of Sciences of the United States of America. 90 (5): 2002–4. Bibcode:1993PNAS...90.2002C. doi:10.1073/pnas.90.5.2002. PMC 46008. PMID 8446622.