APOM

 Apolipoprotein M is a protein that in humans is encoded by the APOM gene.[5][6][7]

APOM
Protein APOM PDB 2WEW.png
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAPOM, G3a, HSPC336, NG20, apo-M, apolipoprotein M
External IDsOMIM606907 MGI1930124 HomoloGene10308 GeneCardsAPOM
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)[1]
Chromosome 6 (human)
Genomic location for APOM
Genomic location for APOM
Band6p21.33Start31,652,416 bp[1]
End31,658,210 bp[1]
RNA expression pattern
PBB GE APOM 214910 s at fs.png

PBB GE APOM 205682 x at fs.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001256169
NM_019101

NM_018816

RefSeq (protein)

NP_001243098
NP_061974

NP_061286

Location (UCSC)Chr 6: 31.65 – 31.66 MbChr 17: 35.13 – 35.13 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
ApoM
Identifiers
SymbolApoM
PfamPF11032
Pfam clanCL0116
InterProIPR022734

The protein encoded by this gene is an apolipoprotein and member of the lipocalin protein family. It is found associated with high density lipoproteins and to a lesser extent with low density lipoproteins and triglyceride-rich lipoproteins. The encoded protein is secreted through the plasma membrane but remains membrane-bound, where it is involved in lipid transport. Two transcript variants encoding two different isoforms have been found for this gene, but only one of them has been fully characterized.[7] The average molecular weight is 21253 Da, and the monoisotopic molecular weight is 21239 Da.

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