This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RBM10-20-RE | 20 (40 μL) | 200 μL |  |
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| RBM10-20-OR | 20 (40 μL) | 200 μL |  |
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| RBM10-20-GO | 20 (40 μL) | 200 μL |  |
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| RBM10-20-GR | 20 (40 μL) | 200 μL |  |
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| RBM10-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]
Gene Symbol : RBM10
Gene Name : RNA binding motif protein 10
Chromosome : CHR X: 471,451,95-471,868,14
Locus : Xp11.3
Alt. Genes : ABI2
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