APOM

APOM
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesAPOM, G3a, HSPC336, NG20, apo-M, apolipoprotein M
External IDsOMIM: 606907; MGI: 1930124; HomoloGene: 10308; GeneCards: APOM; OMA:APOM - orthologs
Orthologs
SpeciesHumanMouse
Entrez

55937

55938

Ensembl

ENSMUSG00000024391

UniProt

O95445

Q9Z1R3

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: 35.35 – 35.35 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse
ApoM
Identifiers
SymbolApoM
PfamPF11032
Pfam clanCL0116
InterProIPR022734
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

Apolipoprotein M is an apolipoprotein and member of the lipocalin protein family that in humans is encoded by the APOM gene. 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. It lacks an external amphipathic motif and is uniquely secreted to plasma without cleavage of its terminal signal peptide. The average molecular weight is 21253 Da, and the monoisotopic molecular weight is 21239 Da.