| Entrez Gene ID | 54875 |
|---|---|
| Official Gene Symbol | CNTLN (GeneCards) |
| Full name | centlein |
| Location | 9p22.2 |
| Other ids | Vega : OTTHUMG00000019599 MIM : 611870 HGNC : HGNC:23432 Ensembl : ENSG00000044459 |
| Other names | C9orf39, C9orf101, bA340N12.1 |
| Summary | None |
Found 7 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 13035 | 54875 | CNTLN | 9 | 17163208 | 17163208 | Asymptomatic | HiSeq X Ten |
| 13316 | 54875 | CNTLN | 9 | 17559435 | 17559435 | Asymptomatic | HiSeq X Ten |
| 13354 | 54875 | CNTLN | 9 | 17181715 | 17181715 | Asymptomatic | HiSeq X Ten |
| 13545 | 54875 | CNTLN | 9 | 17240783 | 17240783 | Asymptomatic | HiSeq X Ten |
| 13698 | 54875 | CNTLN | 9 | 17485749 | 17485749 | Cockayne syndrome | HiSeq X Ten |
| 13719 | 54875 | CNTLN | 9 | 17328555 | 17328555 | Cockayne syndrome | HiSeq X Ten |
| 13753 | 54875 | CNTLN | 9 | 17500148 | 17500148 | Xeroderma Pigmentosum | HiSeq X Ten |