This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SOX14-20-RE | 20 (40 μL) | 200 μL |  |
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| SOX14-20-OR | 20 (40 μL) | 200 μL |  |
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| SOX14-20-GO | 20 (40 μL) | 200 μL |  |
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| SOX14-20-GR | 20 (40 μL) | 200 μL |  |
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| SOX14-20-AQ | 20 (40 μL) | 200 μL |  |
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This intronless gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene are suggested to be responsible for the limb defects associated with blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and Mobius syndrome. [provided by RefSeq, Jul 2008]
Gene Symbol : SOX14
Gene Name : SRY-box 14
Chromosome : CHR 3: 137,764,291-137,766,333
Locus : 3q22.3
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