This gene represents naturally occurring read-through transcription between the neighboring TSNAX (translin-associated factor X) and DISC1 (disrupted in schizophrenia 1) genes on chromosome 1. Alternative splicing results in multiple transcript variants, all of which are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to be protein-coding. These alterations in gene processing may be associated with risk for psychiatric illness, most notably, schizophrenia. [provided by RefSeq, Nov 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TSNAX-DISC1-20-RE | 20 (40 μL) | 200 μL |  |
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| TSNAX-DISC1-20-OR | 20 (40 μL) | 200 μL |  |
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| TSNAX-DISC1-20-GO | 20 (40 μL) | 200 μL |  |
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| TSNAX-DISC1-20-GR | 20 (40 μL) | 200 μL |  |
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| TSNAX-DISC1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene represents naturally occurring read-through transcription between the neighboring TSNAX (translin-associated factor X) and DISC1 (disrupted in schizophrenia 1) genes on chromosome 1. Alternative splicing results in multiple transcript variants, all of which are candidates for nonsense-mediated mRNA decay (NMD) and are unlikely to be protein-coding. These alterations in gene processing may be associated with risk for psychiatric illness, most notably, schizophrenia. [provided by RefSeq, Nov 2010]
Gene Symbol : TSNAX-DISC1
Gene Name : TSNAX-DISC1 readthrough (NMD candidate)
Chromosome : CHR 1: 231,528,652-232,041,271
Locus : 1q42.2
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