This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TBX22-20-RE | 20 (40 μL) | 200 μL |  |
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| TBX22-20-OR | 20 (40 μL) | 200 μL |  |
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| TBX22-20-GO | 20 (40 μL) | 200 μL |  |
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| TBX22-20-GR | 20 (40 μL) | 200 μL |  |
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| TBX22-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Symbol : TBX22
Gene Name : T-box 22
Chromosome : CHR X: 800,147,29-800,358,27
Locus : Xq21.1
Alt. Genes : LRPPRC
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