The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT). [provided by RefSeq, Dec 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TSPYL1-20-RE | 20 (40 μL) | 200 μL |  |
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| TSPYL1-20-OR | 20 (40 μL) | 200 μL |  |
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| TSPYL1-20-GO | 20 (40 μL) | 200 μL |  |
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| TSPYL1-20-GR | 20 (40 μL) | 200 μL |  |
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| TSPYL1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT). [provided by RefSeq, Dec 2009]
Gene Symbol : TSPYL1
Gene Name : TSPY like 1
Chromosome : CHR 6: 116,280,116-116,274,858
Locus : 6q22.1
Alt. Genes : CHST4
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