help  | about  | cite  | software

Gene : APOL2 Homo sapiens

Name  ? apolipoprotein L2 Cytological Location  22q12.3
Brief Description  apolipoprotein L2
Description  This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • AF324224,
  • APOL2,
  • NM_145637,
  • APOL-II,
  • uc003apa.4,
  • APOL-II,
  • apolipoprotein L-II,
  • APOL3,
  • HGNC:619,
  • OTTHUMG00000150634
  • identifiers:
  • 23780,
  • ENSG00000128335,
  • APOL2

Genome feature

Region: gene ? Length: 13746  
Location: 22:36226209-36239954 reverse strand Cyto location: 22q12.3

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

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


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

112 SNPs

5 Cross References

19 Data Sets

22 Homologues

0 Located Features

97 Rna Seq Results