| Entrez Gene ID | 338872 |
|---|---|
| Official Gene Symbol | C1QTNF9 (GeneCards) |
| Full name | C1q and TNF related 9 |
| Location | 13q12.12 |
| Other ids | Vega : OTTHUMG00000016576 MIM : 614285 HGNC : HGNC:28732 Ensembl : ENSG00000240654 |
| Other names | AQL1, CTRP9, C1QTNF9A |
| Summary | None |
Found 4 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 17326 | 338872 | C1QTNF9 | 13 | 24930535 | 24930535 | Asymptomatic | HiSeq X Ten |
| 17861 | 338872 | C1QTNF9 | 13 | 24899269 | 24899269 | Cockayne syndrome | HiSeq X Ten |
| 17986 | 338872 | C1QTNF9 | 13 | 24902545 | 24902545 | Xeroderma Pigmentosum | HiSeq X Ten |
| 27633 | 338872 | C1QTNF9 | 13 | 24985396 | 24985396 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |