This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| USP9X-20-RE | 20 (40 μL) | 200 μL |  |
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| USP9X-20-OR | 20 (40 μL) | 200 μL |  |
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| USP9X-20-GO | 20 (40 μL) | 200 μL |  |
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| USP9X-20-GR | 20 (40 μL) | 200 μL |  |
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| USP9X-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Gene Symbol : USP9X
Gene Name : Ubiquitin specific peptidase 9, X-linked
Chromosome : CHR X: 410,854,19-412,365,78
Locus : Xp11.4
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