Aliases for APOM Gene
External Ids for APOM Gene
Previous GeneCards Identifiers for APOM Gene
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. Alternate splicing results in both coding and non-coding variants of this gene. [provided by RefSeq, Jan 2012]
GeneCards Summary for APOM Gene
APOM (Apolipoprotein M) is a Protein Coding gene. Diseases associated with APOM include Fetal Macrosomia and Huntington Disease-Like 1. Among its related pathways are Metabolism of water-soluble vitamins and cofactors and Signaling by GPCR. Gene Ontology (GO) annotations related to this gene include phospholipid binding and lipid transporter activity.
UniProtKB/Swiss-Prot Summary for APOM Gene
Probably involved in lipid transport. Can bind sphingosine-1-phosphate, myristic acid, palmitic acid and stearic acid, retinol, all-trans-retinoic acid and 9-cis-retinoic acid.