APOA5

APOA5
Identifiers
AliasesAPOA5, APOAV, RAP3, apolipoprotein A5
External IDsOMIM: 606368; MGI: 1913363; HomoloGene: 14197; GeneCards: APOA5; OMA:APOA5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

116519

66113

Ensembl

ENSG00000110243

ENSMUSG00000032079

UniProt

Q6Q788

Q8C7G5

RefSeq (mRNA)

NM_052968
NM_001166598
NM_001371904

NM_080434
NM_001348095

RefSeq (protein)

NP_001160070
NP_443200
NP_001358833

NP_536682
NP_001335024

Location (UCSC)Chr 11: 116.79 – 116.79 MbChr 9: 46.18 – 46.18 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Apolipoprotein A-V is a protein that in humans is encoded by the APOA5 gene on chromosome 11. It is significantly expressed in liver. The protein encoded by this gene is an apolipoprotein and an important determinant of plasma triglyceride levels, a major risk factor for coronary artery disease. It is a component of several lipoprotein fractions including VLDL, HDL, chylomicrons. It is believed that apoA-V affects lipoprotein metabolism by interacting with LDL-R gene family receptors. Considering its association with lipoprotein levels, APOA5 is implicated in metabolic syndrome. The APOA5 gene also contains one of 27 SNPs associated with increased risk of coronary artery disease.