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Gene : APOA5 Homo sapiens

Name  ? apolipoprotein A5 Cytological Location  11q23.3
Brief Description  apolipoprotein A5
Description  The protein encoded by this gene is an apolipoprotein that plays an important role in regulating the plasma triglyceride levels, a major risk factor for coronary artery disease. It is a component of high density lipoprotein and is highly similar to a rat protein that is upregulated in response to liver injury. Mutations in this gene have been associated with hypertriglyceridemia and hyperlipoproteinemia type 5. This gene is located proximal to the apolipoprotein gene cluster on chromosome 11q23. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Oct 2009]
  • synonyms:
  • APOA-V,
  • APOAV,
  • NM_001166598,
  • RAP3,
  • RAP3,
  • uc001ppr.4,
  • apolipoprotein A-V,
  • AF202889,
  • APOA5,
  • HGNC:17288,
  • OTTHUMG00000046116
  • identifiers:
  • 116519,
  • ENSG00000110243,
  • APOA5

Genome feature

Region: gene ? Length: 3054  
Location: 11:116789367-116792420 reverse strand Cyto location: 11q23.3

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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 Structure Displayer

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


2 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.



11 SN Ps

5 Cross References

17 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results