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GeneQ14916272· pop 7· linked from 68 articles

Also known as APO-CII, APOC-II, apolipoprotein C2

protein-coding gene in the species Homo sapiens

Gene data

APOC2
Name
apolipoprotein C2
Type
protein-coding
Aliases
APO-CII, APOC-II

This gene encodes a lipid-binding protein belonging to the apolipoprotein gene family. The protein is secreted in plasma where it is a component of very low density lipoprotein. This protein activates the enzyme lipoprotein lipase, which hydrolyzes triglycerides and thus provides free fatty acids for cells. Mutations in this gene cause hyperlipoproteinemia type IB, characterized by hypertriglyceridemia, xanthomas, and increased risk of pancreatitis and early atherosclerosis. This gene is present in a cluster with other related apolipoprotein genes on chromosome 19. Naturally occurring read-through transcription exists between this gene and the neighboring upstream apolipoprotein C-IV (APOC4) gene. [provided by RefSeq, Mar 2011].

via MyGene.info

Gene · Ensembl

apolipoprotein C2

Symbol
APOC2
Biotype
Protein coding
Organism
Homo sapiens
Location
19:44,936,126-44,949,585
Strand
Forward (+)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Image
Protein APOC2 PDB 1by6.png
Show 5 more facts
HomoloGene ID
47928
genomic start
44946035
genomic end
44949565
cytogenetic location
19q13.32
Sources (7)

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