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Apolipoprotein C2

APOC2
Protein APOC2 PDB 1by6.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases APOC2, APO-CII, APOC-II, apolipoprotein C2
External IDs OMIM: 608083 MGI: 88054 HomoloGene: 47928 GeneCards: APOC2
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000483

NM_001277944
NM_001309795

RefSeq (protein)

NP_000474
NP_000474.2

Location (UCSC) Chr 19: 44.94 – 44.95 Mb Chr 7: 19.67 – 19.68 Mb
PubMed search
Apo-CII
1i5j.jpg
nmr structure of human apolipoprotein c-ii in the presence of sds
Identifiers
Symbol Apo-CII
Pfam PF05355
InterPro IPR008019
SCOP 1by6
SUPERFAMILY 1by6

1SOH, 1BY6, 1I5J, 1O8T

NM_000483

NM_001277944
NM_001309795

NP_000474
NP_000474.2

NP_001296724

Apolipoprotein C2 or apolipoprotein C-II is a protein that in humans is encoded by the APOC2 gene.

The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons. This protein activates the enzyme lipoprotein lipase in capillaries, which hydrolyzes triglycerides and thus provides free fatty acids for cells. Mutations in this gene cause hyperlipoproteinemia type IB, characterized by xanthomas, pancreatitis, and hepatosplenomegaly, but no increased risk for atherosclerosis. Lab tests will show elevated blood levels of triglycerides, cholesterol, and chylomicrons


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