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Gene : FOXC2 Homo sapiens

Name  ? forkhead box C2 Cytological Location  16q24.1
Brief Description  forkhead box C2
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 may play a role in the development of mesenchymal tissues. [provided by RefSeq, Jul 2008]
  • synonyms:
  • uc002fjq.4,
  • MFH-1,
  • FKHL14,
  • forkhead box C2 (MFH-1, mesenchyme forkhead 1),
  • FKHL14,
  • LD,
  • mesenchyme forkhead 1,
  • FOXC2,
  • Y08223,
  • OTTHUMG00000137652,
  • MFH1,
  • MFH-1,
  • NM_005251,
  • HGNC:3801
  • identifiers:
  • 2303,
  • ENSG00000176692,
  • FOXC2

Genome feature

Region: gene ? Length: 2900  
Location: 16:86566829-86569728 Cyto location: 16q24.1

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

118 SN Ps

5 Cross References

17 Data Sets

17 Homologues

0 Located Features

97 Rna Seq Results