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Gene : FOXR1 Homo sapiens

Name  ? forkhead box R1 Cytological Location  11q23.3
Brief Description  forkhead box R1
description  This gene encodes a member of the forkhead box (FOX) family of transcription factors. FOX family members are monomeric, helix-turn-helix proteins with a core DNA-binding domain of approximately 110 aa. Many FOX transcription factors play roles in determining cell fates during early development. This forkhead box protein lacks the C-terminal basic region found in many other FOX family members. It is located within the 11q23.3 region which is commonly deleted in neuroblastomas. [provided by RefSeq, Jul 2008]
  • synonyms:
  • DLNB13,
  • DLNB13,
  • AB094092,
  • FOXN5,
  • OTTHUMG00000166347,
  • HGNC:29980,
  • uc001pui.4,
  • FOXN5,
  • FOXR1,
  • NM_181721
  • identifiers:
  • 283150,
  • ENSG00000176302,
  • FOXR1

Genome feature

Region: gene ? Length: 10204  
Location: 11:118971398-118981601 Cyto location: 11q23.3


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Function

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0 Pathways

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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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

0 SN Ps

5 Cross References

12 Data Sets

5 Homologues

0 Located Features

90 Rna Seq Results