| Entrez gene ID | | 2296 |
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| Official gene symbol | | FOXC1 |
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| Full name | | forkhead box C1 |
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| Aliases | | ,ARA,FKHL7,FREAC-3,FREAC3,IGDA,IHG1,IRID1,RIEG3, |
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| Gene summary | | 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] |
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| Location | | Chromosome: 6 Locus: 6p25 |
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| Gene position | | 1610681 - 1614132 Map Viewer |
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| Gene orientation | | plus |
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| Gene size | | 3452 bp |
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| Gene sequence |
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| OMIM ID | | 601090 |
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