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- accession：NM_001453
- 基因别名：FOXC1
- 基因描述：Homo sapiens forkhead box C1 (FOXC1), mRNA.
- 载体：现货载体
- CDS区长度：1662
- 翻译后氨基酸长度：553
- 基因简介：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]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
