| Entrez Gene ID | 10144 |
|---|---|
| Official Gene Symbol | FAM13A (GeneCards) |
| Full name | family with sequence similarity 13 member A |
| Location | 4q22.1 |
| Other ids | Vega : OTTHUMG00000161006 MIM : 613299 HGNC : HGNC:19367 Ensembl : ENSG00000138640 |
| Other names | FAM13A1, ARHGAP48 |
| Summary | None |
Found 5 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 6395 | 10144 | FAM13A | 4 | 89962284 | 89962284 | Asymptomatic | HiSeq X Ten |
| 6728 | 10144 | FAM13A | 4 | 89869981 | 89869981 | Asymptomatic | HiSeq X Ten |
| 7206 | 10144 | FAM13A | 4 | 89665643 | 89665643 | Cockayne syndrome | HiSeq X Ten |
| 7207 | 10144 | FAM13A | 4 | 89869070 | 89869070 | Cockayne syndrome | HiSeq X Ten |
| 22941 | 10144 | FAM13A | 4 | 89705120 | 89705120 | Asymptomatic | HiSeq X Ten Single cell Sequencing Cell cloning |