Apolipoprotein C2

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

APOC2
Protein APOC2 PDB 1by6.png
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAPOC2, APO-CII, APOC-II, apolipoprotein C2
External IDsOMIM608083 MGI88054 HomoloGene47928 GeneCardsAPOC2
Gene location (Human)
Chromosome 19 (human)
Chr.Chromosome 19 (human)[1]
Chromosome 19 (human)
Genomic location for APOC2
Genomic location for APOC2
Band19q13.32Start44,945,971 bp[1]
End44,949,566 bp[1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000483

NM_001277944
NM_001309795

RefSeq (protein)

NP_000474
NP_000474.2

NP_001296728
NP_001264873
NP_001296724

Location (UCSC)Chr 19: 44.95 – 44.95 MbChr 7: 19.67 – 19.68 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Apo-CII
1i5j.jpg
nmr structure of human apolipoprotein c-ii in the presence of sds
Identifiers
SymbolApo-CII
PfamPF05355
InterProIPR008019
SCOP21by6 / SCOPe / SUPFAM

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,[5] which hydrolyzes triglycerides and thus provides free fatty acids for cells. Mutations in this gene cause hyperlipoproteinemia type IB, characterized by xanthomaspancreatitis, and hepatosplenomegaly, but no increased risk for atherosclerosis. Lab tests will show elevated blood levels of triglycerides, cholesterol, and chylomicrons[6]

This article uses material from the Wikipedia article
 Metasyntactic variable, which is released under the 
Creative Commons
Attribution-ShareAlike 3.0 Unported License
.