The following FOXC1 gene sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the FOXC1 gene which is encoded by the open reading frame (ORF) sequence. ORF sequences can be delivered in our standard vector, pcDNA3.1+/C-(K)DYK or the vector of your choice as an expression/transfection-ready ORF clone. Not the clone you want? Click here to find your clone.
||Documents for ORF clone product in dufault vector
||ORF Nucleotide Sequence (Length: 1662bp)
||pcDNA3.1+/C-(K)DYK or customized vector
|Tag on pcDNA3.1+/C-(K)DYK
||C terminal DYKDDDDK tags
|ORF Insert Method
||CloneEZ® Seamless cloning technology
||Homo sapiens (human)
||forkhead box protein C1
||REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from AL034344.24.
This sequence is a reference standard in the RefSeqGene project.
On Dec 14, 2006 this sequence version replaced gi:4503734.
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, Jul 2008].
Sequence Note: This RefSeq record was created from genomic sequence
data because mRNA transcripts were not available for the full
length of the gene. The extent of this transcript is supported by
orthologous mouse data.
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
COMPLETENESS: complete on the 3' end.