Entrez Gene ID | 79632 |
---|---|
Official Gene Symbol | FAM184A (GeneCards) |
Full name | family with sequence similarity 184 member A |
Location | 6q22.31 |
Other ids | Vega : OTTHUMG00000015471 HGNC : HGNC:20991 Ensembl : ENSG00000111879 |
Other names | C6orf60 |
Summary | None |
Found 4 variants in this database.
Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
---|---|---|---|---|---|---|---|
9470 | 79632 | FAM184A | 6 | 119379781 | 119379781 | Asymptomatic | HiSeq X Ten |
10054 | 79632 | FAM184A | 6 | 119340946 | 119340946 | Cockayne syndrome | HiSeq X Ten |
10165 | 79632 | FAM184A | 6 | 119342230 | 119342230 | Cockayne syndrome | HiSeq X Ten |
10223 | 79632 | FAM184A | 6 | 119471634 | 119471634 | Cockayne syndrome | HiSeq X Ten |