| Entrez Gene ID | 2534 |
|---|---|
| Official Gene Symbol | FYN (GeneCards) |
| Full name | FYN proto-oncogene, Src family tyrosine kinase |
| Location | 6q21 |
| Other ids | Vega : OTTHUMG00000016305 MIM : 137025 HGNC : HGNC:4037 Ensembl : ENSG00000010810 |
| Other names | SLK, SYN, p59-FYN |
| Summary | This gene is a member of the protein-tyrosine kinase oncogene family. It encodes a membrane-associated tyrosine kinase that has been implicated in the control of cell growth. The protein associates with the p85 subunit of phosphatidylinositol 3-kinase and interacts with the fyn-binding protein. Alternatively spliced transcript variants encoding distinct isoforms exist. [provided by RefSeq, Jul 2008] |
Found 6 variants in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 1374 | 2534 | FYN | 6 | 112015899 | 112015899 | Autism Spectrum Disorders | NextSeq500 v2 |
| 1375 | 2534 | FYN | 6 | 112015899 | 112015899 | Autism Spectrum Disorders | NextSeq500 v2 |
| 9032 | 2534 | FYN | 6 | 112339949 | 112339949 | Asymptomatic | NextSeq500 v2 HiSeq 2000 |
| 9090 | 2534 | FYN | 6 | 112115907 | 112115907 | Asymptomatic | NextSeq500 v2 HiSeq 2000 HiSeq X Ten |
| 29148 | 2534 | FYN | 6 | 112015899 | 112015899 | Autism Spectrum Disorders | NextSeq500 v2 HiSeq 2000 HiSeq X Ten PASM |
| 29791 | 2534 | FYN | 6 | 112015899 | 112015899 | Autism Spectrum Disorders | NextSeq500 v2 HiSeq 2000 HiSeq X Ten PASM NextSeq500 |