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
|
|
GO accession | Term name | Evidence code | Go category |
---|
|
|
|
|
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 |
|
|
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 |
|