| Entrez Gene ID | 160313 |
|---|---|
| Official Gene Symbol | KRT19P2 (GeneCards) |
| Full name | keratin 19 pseudogene 2 |
| Location | 12q22 |
| Other ids | HGNC : HGNC:33423 Ensembl : ENSG00000216306 |
| Other names | KRT19P5 |
| Summary | None |
Found 6 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 16778 | 160313 | KRT19P2 | 12 | 95258462 | 95258462 | Asymptomatic | HiSeq X Ten |
| 16779 | 160313 | KRT19P2 | 12 | 95278574 | 95278574 | Asymptomatic | HiSeq X Ten |
| 16974 | 160313 | KRT19P2 | 12 | 95239351 | 95239351 | Cockayne syndrome | HiSeq X Ten |
| 17049 | 160313 | KRT19P2 | 12 | 95238704 | 95238704 | Xeroderma Pigmentosum | HiSeq X Ten |
| 17050 | 160313 | KRT19P2 | 12 | 95238705 | 95238705 | Xeroderma Pigmentosum | HiSeq X Ten |
| 27489 | 160313 | KRT19P2 | 12 | 95253888 | 95253888 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |