This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SOX2-20-RE | 20 (40 μL) | 200 μL |  |
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| SOX2-20-OR | 20 (40 μL) | 200 μL |  |
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| SOX2-20-GO | 20 (40 μL) | 200 μL |  |
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| SOX2-20-GR | 20 (40 μL) | 200 μL |  |
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| SOX2-20-AQ | 20 (40 μL) | 200 μL |  |
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This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008]
Gene Symbol : SOX2
Gene Name : SRY-box 2
Chromosome : CHR 3: 181,711,923-181,714,435
Locus : 3q26.33
Alt. Genes : LRPPRC
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