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Gene : FOXC1 Homo sapiens

Name  ? forkhead box C1 Cytological Location  6p25.3
Brief Description  forkhead box C1
Description  This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly. [provided by RefSeq, Jul 2008]
  • synonyms:
  • IHG1,
  • IHG1,
  • AF048693,
  • FREAC-3,
  • IRID1,
  • FREAC3,
  • IRID1,
  • NM_001453,
  • IGDA,
  • FREAC3,
  • RIEG3,
  • HGNC:3800,
  • FKHL7,
  • ARA,
  • FOXC1,
  • ARA,
  • FKHL7,
  • IGDA,
  • uc003mtp.4,
  • OTTHUMG00000016182,
  • ASGD3
  • identifiers:
  • 2296,
  • ENSG00000054598,
  • FOXC1

Genome feature

Region: gene ? Length: 3983  
Location: 6:1609915-1613897 Cyto location: 6p25.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


2 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


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

Gene Ontology

Gene --> GO terms.



0 Pathways

222 SN Ps

5 Cross References

19 Data Sets

19 Homologues

0 Located Features

97 Rna Seq Results