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Gene id 2534
Gene Summary    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed    

Gene Summary

Gene Symbol FYN   Gene   UCSC   Ensembl
Aliases SLK, SYN, p59-FYN
Gene name FYN proto-oncogene, Src family tyrosine kinase
Alternate names tyrosine-protein kinase Fyn, FYN oncogene related to SRC, FGR, YES, OKT3-induced calcium influx regulator, c-syn protooncogene, proto-oncogene Syn, proto-oncogene c-Fyn, src-like kinase, src/yes-related novel, tyrosine kinase p59fyn(T),
Gene location 6q21 (111873451: 111660331)     Exons: 19     NC_000006.12
Gene summary(Entrez) 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
OMIM 137025

Protein Summary

Gene ontology

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GO accessionTerm nameEvidence codeGo category

KEGG pathways

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Pathway idPathway name
hsa00190Oxidative phosphorylation
hsa00072Synthesis and degradation of ketone bodies
hsa00270Cysteine and methionine metabolism
hsa00310Lysine degradation
hsa00380Tryptophan metabolism
hsa00480Glutathione metabolism
hsa00604Glycosphingolipid biosynthesis - ganglio series
hsa00860Porphyrin and chlorophyll metabolism
hsa03060Protein export
hsa04141Protein processing in endoplasmic reticulum
hsa04141Protein processing in endoplasmic reticulum
hsa04010MAPK signaling pathway
hsa04010MAPK signaling pathway
hsa04012ErbB signaling pathway
hsa04072Phospholipase D signaling pathway
hsa04071Sphingolipid signaling pathway
hsa04510Focal adhesion
hsa04520Adherens junction
hsa04611Platelet activation
hsa04650Natural killer cell mediated cytotoxicity
hsa04660T cell receptor signaling pathway
hsa04664Fc epsilon RI signaling pathway
hsa04725Cholinergic synapse
hsa04360Axon guidance
hsa04380Osteoclast differentiation
hsa05020Prion diseases
hsa05416Viral myocarditis
hsa05130Pathogenic Escherichia coli infection
Associated diseases References
Arterial hypertension GAD: 17334644
Cleft defects GAD: 18978678
Alzheimer's disease GAD: 15082191
Parkinson disease GAD: 18628988
Bipolar disorder GAD: 19330793
Schizophrenia GAD: 11121167
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Plays a role in spermatogenesis and development of testicular germ cells MIK: 11944913
Teratozoospermia MIK: 17327269
Unexplained infertility MIK: 25753583

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
11944913 Plays a ro
le in sper
matogenesi
s and deve
lopment of
testicula
r germ cel
ls


Male infertility
Show abstract
17327269 Teratozoos
permia

19 (6 controls
, 13 cases)
Male infertility GSE6872 analyzed by GEO2R (cutoff 1.5 fold)
Show abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract
25753583 Unexplaine
d infertil
ity

46 (17 fertile
men, 29 male pa
tients)
Male infertility Microarray
Show abstract