FYN Gene: Structure, Function, and Clinical Significance

A comprehensive overview of the FYN proto-oncogene, a Src family tyrosine kinase involved in cell signaling, cancer, and neurological disorders.

Gene Information Card

Symbol FYN
Full Name FYN proto-oncogene, Src family tyrosine kinase
Gene Type protein coding
Chromosomal Location 6q21
NCBI Gene ID 2534 ncbi.nlm.nih.gov/gene/2534
Ensembl ID ENSG00000110848
UniProt ID P06241
OMIM ID 137025
HGNC ID 4037
Aliases SLK, SYN, p59-FYN

Description

The FYN gene encodes a non-receptor tyrosine kinase belonging to the Src family. It is involved in various cellular processes including cell growth, adhesion, and immune signaling. FYN is expressed in multiple tissues, with high levels in the brain, and plays roles in T-cell receptor signaling and neuronal function. Aberrant FYN activity has been linked to cancers and neurodegenerative diseases.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Prostate Cancer FYN overexpression and activation promote tumor progression and metastasis Multiple studies (e.g., PMID: 23455172) show elevated FYN in prostate cancer tissues and cell lines
Glioblastoma FYN signaling contributes to cell migration and invasion COSMIC and literature reports indicate FYN alterations in glioblastoma
Alzheimer's Disease FYN phosphorylates tau protein, contributing to neurofibrillary tangles Evidence from animal models and human brain studies (e.g., PMID: 21867817)
T-cell Acute Lymphoblastic Leukemia (T-ALL) FYN mutations or overexpression enhance T-cell signaling COSMIC lists FYN mutations in T-ALL samples
Melanoma FYN activation promotes cell survival and proliferation Studies show FYN is overexpressed in melanoma cell lines (e.g., PMID: 21317931)

Expression Profile

Tissue Expression
Tissue nTPM level
Brain High nTPM ~ 50-100 (varies by region)
Lymphoid tissues Moderate nTPM ~ 20-40
Lung Low nTPM ~ 10-20
Liver Low nTPM ~ 5-10
Kidney Low nTPM ~ 5-10
Cell Line Expression
Cell Line nTPM Notes
K-562 (leukemia) High nTPM ~ 80
MCF7 (breast cancer) Moderate nTPM ~ 30
A549 (lung cancer) Low nTPM ~ 15
HEK293 (embryonic kidney) Moderate nTPM ~ 25
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
p.Leu174Phe Missense Rare (<0.1%) Potential gain-of-function in kinase activity
p.Arg176Cys Missense Rare (<0.1%) Unknown functional effect
p.Thr343Met Missense Rare (<0.1%) May affect kinase domain stability
p.Pro250Leu Missense Rare (<0.1%) Reported in cancer samples (COSMIC)
Mutation functional classification

Loss of Function (LOF)

Not well documented; some mutations may reduce kinase activity but no clear loss-of-function phenotype.

Gain of Function (GOF)

Several missense mutations in the kinase domain are predicted to increase activity, promoting oncogenic signaling.

Dominant Negative (DN)

Not reported for FYN.

Gene Ontology (GO)

• protein tyrosine kinase activity • ATP binding
• signal transduction • cell adhesion
• T cell receptor signaling pathway • neuron projection development

Pathways

T cell receptor signaling pathway
Fc epsilon RI signaling pathway
Neurotrophin signaling pathway
Integrin signaling pathway
ErbB signaling pathway

Protein Summary

FYN is a 59 kDa non-receptor tyrosine kinase that localizes to the plasma membrane via myristoylation and palmitoylation. It contains SH3, SH2, and kinase domains. FYN is activated by dephosphorylation of a C-terminal inhibitory tyrosine (Y531) and autophosphorylation of Y420. It interacts with multiple adaptor proteins and receptors, regulating cytoskeletal dynamics, cell survival, and differentiation. In the brain, FYN modulates NMDA receptor function and tau phosphorylation.

Related Products

Product name Cat.No. Species Gene ID
FYN Knockout HEK293 Cell Line EDJ-KQ17821 Human 2534 Details Get a Quote
FYN Knockout A-549 Cell Line EDJ-KQ21526 Human 2534 Details Get a Quote
FYN Knockout HCT 116 Cell Line EDJ-KQ21527 Human 2534 Details Get a Quote
FYN Knockout HeLa Cell Line EDJ-KQ21528 Human 2534 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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