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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FOXC1-20-RE | 20 (40 μL) | 200 μL |  |
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| FOXC1-20-OR | 20 (40 μL) | 200 μL |  |
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| FOXC1-20-GO | 20 (40 μL) | 200 μL |  |
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| FOXC1-20-GR | 20 (40 μL) | 200 μL |  |
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| FOXC1-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : FOXC1
Gene Name : Forkhead box C1
Chromosome : CHR 6: 161,044,5-161,389,6
Locus : 6p25.3
Alt. Genes : CFM1
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