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Gene : APOM Homo sapiens

Name  ? apolipoprotein M Cytological Location  6p21.33
Brief Description  apolipoprotein M
Description  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]
  • synonyms:
  • AJ245434,
  • HGNC:13916,
  • uc003nvl.4,
  • NG20,
  • APOM,
  • OTTHUMG00000031250,
  • apo-M,
  • G3a,
  • NG20,
  • HSPC336,
  • G3a,
  • NM_019101
  • identifiers:
  • 55937,
  • ENSG00000204444,
  • APOM

Genome feature

Region: gene ? Length: 5807  
Location: 6:31652404-31658210 Cyto location: 6p21.33

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Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3740 SN Ps

5 Cross References

14 Data Sets

2 Homologues

0 Located Features

97 Rna Seq Results