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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:
  • OTTHUMG00000150634,
  • APOL2,
  • NM_145637,
  • apolipoprotein L-II,
  • uc003apa.4,
  • AF324224,
  • HGNC:619,
  • APOL-II,
  • APOL3,
  • APOL-II
  • identifiers:
  • 23780,
  • ENSG00000128335,
  • APOL2

Genome feature

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


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Function

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0 Pathways

Gene --> GO terms.

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

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

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 Pathways

42 SN Ps

5 Cross References

16 Data Sets

24 Homologues

0 Located Features

90 Rna Seq Results