APOA2

 Apolipoprotein A-II is a protein that in humans is encoded by the APOA2 gene.[5]

APOA2
Protein APOA2 PDB 1l6l.png
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAPOA2, Apo-AII, ApoA-II, apoAII, Apolipoprotein A2
External IDsMGI88050 HomoloGene1242 GeneCardsAPOA2
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)[1]
Chromosome 1 (human)
Genomic location for APOA2
Genomic location for APOA2
Band1q23.3Start161,222,292 bp[1]
End161,223,631 bp[1]
RNA expression pattern
PBB GE APOA2 219465 at fs.png

PBB GE APOA2 219466 s at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001643

NM_013474
NM_001305549
NM_001305550
NM_001305585

RefSeq (protein)

NP_001634

NP_001292478
NP_001292479
NP_001292514
NP_038502

Location (UCSC)Chr 1: 161.22 – 161.22 MbChr 1: 171.23 – 171.23 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
ApoA-II
PDB 1l6l EBI.jpg
structures of apolipoprotein a-ii and a lipid surrogate complex provide insights into apolipoprotein-lipid interactions
Identifiers
SymbolApoA-II
PfamPF04711
InterProIPR006801
SCOP21l6k / SCOPe / SUPFAM

FunctionEdit

This gene encodes apolipoprotein (apo-) A-II, which is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. Defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia.[6]

InteractionsEdit

APOA2 has been shown to interact with PLTP.[7]

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