APOM

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Apolipoprotein M is an apolipoprotein and member of the lipocalin protein family that in humans is encoded by the APOM gene.[5][6][7] 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] It lacks an external amphipathic motif and is uniquely secreted to plasma without cleavage of its terminal signal peptide.[8] The average molecular weight is 21253 Da, and the monoisotopic molecular weight is 21239 Da.

PDBOrtholog search: PDBe RCSB
AliasesAPOM, G3a, HSPC336, NG20, apo-M, apolipoprotein M
Quick facts Available structures, PDB ...
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
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: 35.35 – 35.35 Mb
PubMed search[3][4]
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Quick facts Identifiers, Symbol ...
ApoM
Identifiers
SymbolApoM
PfamPF11032
Pfam clanCL0116
InterProIPR022734
Available protein structures:
PDB  IPR022734 PF11032 (ECOD; PDBsum)  
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