The following SIX1 gene sequences were retrieved from the NCBI Reference Sequence Database (RefSeq). These sequences represent the protein coding region of the SIX1 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: 855bp)
||pcDNA3.1+/C-(K)DYK or customized vector
||Document: User manual_GenEZ ORF Clone Products.pdf (pdf)
|Tag on pcDNA3.1+/C-(K)DYK
||C terminal DYKDDDDK tags
||Document: MSDS_GenEZ ORF Clone Products.pdf (pdf)
|ORF Insert Method
||CloneEZ® Seamless cloning technology
||Homo sapiens (human)
||homeobox protein SIX1
||REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BC008874.2, X91868.1 and
This sequence is a reference standard in the RefSeqGene project.
On Apr 29, 2008 this sequence version replaced gi:142345106.
Summary: The protein encoded by this gene is a homeobox protein
that is similar to the Drosophila 'sine oculis' gene product. This
gene is found in a cluster of related genes on chromosome 14 and is
thought to be involved in limb development. Defects in this gene
are a cause of autosomal dominant deafness type 23 (DFNA23) and
branchiootic syndrome type 3 (BOS3). [provided by RefSeq, Jul
Sequence Note: This RefSeq record was created from transcript and
genomic sequence data because no single transcript was available
for the full length of the gene. The extent of this transcript is
supported by transcript alignments.
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.
Transcript exon combination :: BC008874.2, X91868.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
COMPLETENESS: complete on the 3' end.