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Gene : FOXO3 Homo sapiens

Name  ? forkhead box O3 Cytological Location  6q21
Brief Description  forkhead box O3
Description  This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. This gene likely functions as a trigger for apoptosis through expression of genes necessary for cell death. Translocation of this gene with the MLL gene is associated with secondary acute leukemia. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]
  • synonyms:
  • FOXO3A,
  • AF032886,
  • FOXO3,
  • FKHRL1,
  • HGNC:3821,
  • FKHRL1,
  • OTTHUMG00000015327,
  • AF6q21,
  • FOXO2,
  • FOXO2,
  • FOXO3A,
  • FKHRL1P2,
  • AF6q21,
  • uc003psk.3,
  • NM_001455
  • identifiers:
  • 2309,
  • ENSG00000118689,
  • FOXO3

Genome feature

Region: gene ? Length: 124950  
Location: 6:108559825-108684774 Cyto location: 6q21


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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

0 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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Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

166 SN Ps

5 Cross References

18 Data Sets

6 Homologues

10 Located Features

97 Rna Seq Results