Gene Gene information from NCBI Gene database.
Entrez ID 2534
Gene name FYN proto-oncogene, Src family tyrosine kinase
Gene symbol FYN
Synonyms (NCBI Gene)
SLKSYNp59-FYN
Chromosome 6
Chromosome location 6q21
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
miRNA miRNA information provided by mirtarbase database.
33
miRTarBase ID miRNA Experiments Reference
MIRT022048 hsa-miR-128-3p Microarray 17612493
MIRT038910 hsa-miR-93-3p CLASH 23622248
MIRT437821 hsa-miR-125a-3p Luciferase reporter assay 23606749
MIRT437821 hsa-miR-125a-3p Luciferase reporter assay 23606749
MIRT699208 hsa-miR-5580-3p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
176
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000304 Process Response to singlet oxygen IEA
GO:0000304 Process Response to singlet oxygen ISS 27525436
GO:0001664 Function G protein-coupled receptor binding IEA
GO:0001664 Function G protein-coupled receptor binding IPI 23169819
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
137025 4037 ENSG00000010810
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P06241
Protein name Tyrosine-protein kinase Fyn (EC 2.7.10.2) (Proto-oncogene Syn) (Proto-oncogene c-Fyn) (Src-like kinase) (SLK) (p59-Fyn)
Protein function Non-receptor tyrosine-protein kinase that plays a role in many biological processes including regulation of cell growth and survival, cell adhesion, integrin-mediated signaling, cytoskeletal remodeling, cell motility, immune response and axon gu
PDB 1A0N , 1AOT , 1AOU , 1AVZ , 1AZG , 1EFN , 1FYN , 1G83 , 1M27 , 1NYF , 1NYG , 1SHF , 1ZBJ , 2DQ7 , 2MQI , 2MRJ , 2MRK , 3H0F , 3H0H , 3H0I , 3UA6 , 3UA7 , 4D8D , 4EIK , 4U17 , 4U1P , 4ZNX , 5ZAU , 6EDF , 6IPY , 6IPZ , 7A2J , 7A2K , 7A2L , 7A2M , 7A2N , 7A2O , 7A2P , 7A2Q , 7A2R , 7A2S , 7A2T , 7A2U , 7A2V , 7A2W , 7A2X , 7A2Y , 7A2Z , 7UD6 , 8KDX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00018 SH3_1 88 135 SH3 domain Domain
PF00017 SH2 149 231 SH2 domain Domain
PF07714 PK_Tyr_Ser-Thr 271 520 Protein tyrosine and serine/threonine kinase Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 1 is highly expressed in the brain. Isoform 2 is expressed in cells of hemopoietic lineages, especially T-lymphocytes. {ECO:0000269|PubMed:10196263}.
Sequence
Sequence length 537
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
EBV-positive nodal T- and NK-cell lymphoma Pathogenic rs1351655525, rs370573757 RCV004560282
RCV004560283
RCV004560284
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Premature ovarian failure Uncertain significance rs1800846906 RCV001270202
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acquired Immunodeficiency Syndrome Inhibit 8823293
Adenocarcinoma of Lung Associate 29266838
Alzheimer Disease Associate 22927204, 28033507, 32751526, 35563596, 36258016
Aneuploidy Associate 19404734
Arthritis Rheumatoid Associate 33430905
Ataxia Telangiectasia Associate 11315256
Autistic Disorder Associate 36039581
Bone Resorption Associate 9844106
Breast Neoplasms Associate 19404734, 21480388, 37958964
Calcinosis Cutis Associate 26493492