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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:
  • OTTHUMG00000046116,
  • APOA5,
  • NM_001166598,
  • uc001ppr.4,
  • APOAV,
  • apolipoprotein A-V,
  • RAP3,
  • AF202889,
  • HGNC:17288,
  • RAP3,
  • APOA-V
  • identifiers:
  • 116519,
  • ENSG00000110243,
  • APOA5

Genome feature

Region: gene ? Length: 3051  
Location: 11:116789370-116792420 reverse strand Cyto location: 11q23.3


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 SN Ps

5 Cross References

17 Data Sets

10 Homologues

0 Located Features

90 Rna Seq Results