| Entrez Gene ID | 100303453 |
|---|---|
| Official Gene Symbol | TSNAX-DISC1 (GeneCards) |
| Full name | TSNAX-DISC1 readthrough (NMD candidate) |
| Location | 1q42.2 |
| Other ids | Vega : OTTHUMG00000183905 HGNC : HGNC:49177 Ensembl : ENSG00000270106 |
| Other names | None |
| Summary | 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] |
Found 9 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 1624 | 100303453 | TSNAX-DISC1 | 1 | 232114594 | 232114594 | Asymptomatic | HiSeq X Ten |
| 2277 | 100303453 | TSNAX-DISC1 | 1 | 232396285 | 232396285 | Asymptomatic | HiSeq X Ten |
| 2547 | 100303453 | TSNAX-DISC1 | 1 | 231696251 | 231696251 | Asymptomatic | HiSeq X Ten |
| 2574 | 100303453 | TSNAX-DISC1 | 1 | 231980039 | 231980039 | Asymptomatic | HiSeq X Ten |
| 2613 | 100303453 | TSNAX-DISC1 | 1 | 232379338 | 232379338 | Asymptomatic | HiSeq X Ten |
| 2660 | 100303453 | TSNAX-DISC1 | 1 | 232513754 | 232513754 | Cockayne syndrome | HiSeq X Ten |
| 2708 | 100303453 | TSNAX-DISC1 | 1 | 232121940 | 232121940 | Cockayne syndrome | HiSeq X Ten |
| 2780 | 100303453 | TSNAX-DISC1 | 1 | 232428734 | 232428734 | Xeroderma Pigmentosum | HiSeq X Ten |
| 24449 | 100303453 | TSNAX-DISC1 | 1 | 231822585 | 231822585 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |