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Gene : APOL4 Homo sapiens

Name  ? apolipoprotein L4 Cytological Location  22q12.3
Brief Description  apolipoprotein L4
description  The protein encoded by this gene is a member of the apolipoprotein L family and may play a role in lipid exchange and transport throughout the body, as well as in reverse cholesterol transport from peripheral cells to the liver. Two transcript variants encoding two different isoforms have been found for this gene. Only one of the isoforms appears to be a secreted protein. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000150630,
  • AF305226,
  • APOL4,
  • NM_145660,
  • HGNC:14867,
  • APOL-IV,
  • uc032qnf.2
  • identifiers:
  • 80832,
  • ENSG00000100336,
  • APOL4

Genome feature

Region: gene ? Length: 15706  
Location: 22:36189128-36204833 reverse strand Cyto location: 22q12.3

Uni Prot Comments Displayer

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Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer

Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

2011 SN Ps

5 Cross References

16 Data Sets

24 Homologues

0 Located Features

90 Rna Seq Results