| Entrez Gene ID | 338811 |
|---|---|
| Official Gene Symbol | FAM19A2 (GeneCards) |
| Full name | family with sequence similarity 19 member A2, C-C motif chemokine like |
| Location | 12q14.1 |
| Other ids | Vega : OTTHUMG00000170207 MIM : 617496 HGNC : HGNC:21589 Ensembl : ENSG00000198673 |
| Other names | TAFA2, TAFA-2 |
| Summary | This gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP-1alpha, a member of the CC-chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain-specific chemokines or neurokines, that act as regulators of immune and nervous cells. [provided by RefSeq, Jul 2008] |
Found 9 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 16058 | 338811 | FAM19A2 | 12 | 62416793 | 62416793 | Asymptomatic | HiSeq X Ten |
| 16519 | 338811 | FAM19A2 | 12 | 62432075 | 62432075 | Asymptomatic | HiSeq X Ten |
| 16529 | 338811 | FAM19A2 | 12 | 62284789 | 62284789 | Asymptomatic | HiSeq X Ten |
| 16659 | 338811 | FAM19A2 | 12 | 62550011 | 62550011 | Asymptomatic | HiSeq X Ten |
| 16938 | 338811 | FAM19A2 | 12 | 62422633 | 62422633 | Cockayne syndrome | HiSeq X Ten |
| 16957 | 338811 | FAM19A2 | 12 | 62190936 | 62190936 | Cockayne syndrome | HiSeq X Ten |
| 16979 | 338811 | FAM19A2 | 12 | 62536344 | 62536344 | Cockayne syndrome | HiSeq X Ten |
| 16982 | 338811 | FAM19A2 | 12 | 62208127 | 62208127 | Cockayne syndrome | HiSeq X Ten |
| 17030 | 338811 | FAM19A2 | 12 | 62358228 | 62358228 | Xeroderma Pigmentosum | HiSeq X Ten |