LYN Gene (LYN Proto-Oncogene, Src Family Tyrosine Kinase)

Comprehensive biomedical resource for LYN gene: function, expression, mutations, and associated diseases.

Gene Information Card

Symbol LYN
Full Name LYN proto-oncogene, Src family tyrosine kinase
Gene Type protein-coding
Chromosomal Location 8q12.1
NCBI Gene ID 4067 ncbi.nlm.nih.gov/gene/4067
Ensembl ID ENSG00000254087
UniProt ID P07948
OMIM ID 165120
HGNC ID 6735
Aliases JTK8, p53Lyn, p56Lyn

Description

LYN encodes a member of the Src family of non-receptor tyrosine kinases. It is widely expressed in hematopoietic cells, neural tissues, and various epithelial cells. LYN functions as a critical regulator of immune receptor signaling, cell proliferation, differentiation, and apoptosis. Aberrant LYN activity is implicated in hematologic malignancies, autoimmune disorders, and solid tumors.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Chronic myeloid leukemia (CML) LYN overexpression and constitutive activation contribute to BCR-ABL-independent resistance to tyrosine kinase inhibitors. PMID: 15692054; COSMIC
Acute myeloid leukemia (AML) Activating mutations and increased LYN kinase activity promote leukemogenesis. PMID: 23327922; ClinVar
Systemic lupus erythematosus (SLE) LYN deficiency or altered signaling disrupts B-cell tolerance and enhances autoantibody production. PMID: 15356147; OMIM
Breast cancer LYN overexpression correlates with poor prognosis and promotes invasion and metastasis. PMID: 16980330; COSMIC
Colorectal cancer LYN activation via Src family kinase signaling enhances tumor growth and migration. PMID: 21502544; COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Spleen 45.2 High
Lymph node 38.7 High
Bone marrow 32.1 High
Whole blood 28.5 High
Brain (cerebellum) 12.3 Medium
Lung 8.9 Low
Liver 4.2 Low
Cell Line Expression
Cell Line nTPM Notes
K-562 (CML) 62.4 High expression; BCR-ABL positive
HL-60 (AML) 55.1 High expression
Raji (Burkitt lymphoma) 48.7 High expression
MCF7 (breast cancer) 18.3 Medium expression
HEK293 (embryonic kidney) 6.5 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1169A>G (p.Tyr390Cys) Missense <1% (COSMIC) Gain-of-function; increased kinase activity
c.1280G>A (p.Arg427Gln) Missense <1% (COSMIC) Unknown; located in kinase domain
c.1666C>T (p.Arg556*) Nonsense <0.1% (ClinVar) Loss-of-function; truncated protein
c.1522G>A (p.Glu508Lys) Missense <0.5% (COSMIC) Gain-of-function; enhanced signaling
Mutation functional classification

Loss of Function (LOF)

Nonsense mutations (e.g., p.Arg556*) and some missense variants that disrupt kinase activity or protein stability lead to reduced LYN function, associated with autoimmune phenotypes.

Gain of Function (GOF)

Missense mutations in the kinase domain (e.g., p.Tyr390Cys, p.Glu508Lys) increase catalytic activity, promoting oncogenic signaling in hematologic malignancies.

Dominant Negative (DN)

No well-characterized dominant-negative mutations reported for LYN.

Gene Ontology (GO)

• GO:0004715 • non-membrane spanning protein tyrosine kinase activity
• GO:0005524 • ATP binding
• GO:0005737 • cytoplasm
• GO:0005886 • plasma membrane
• GO:0007169 • transmembrane receptor protein tyrosine kinase signaling pathway
• GO:0038096 • Fc-gamma receptor signaling pathway involved in phagocytosis
• GO:0045087 • innate immune response
• GO:0050852 • T cell receptor signaling pathway

Pathways

B cell receptor signaling pathway (KEGG: hsa04662)
Fc gamma R-mediated phagocytosis (KEGG: hsa04666)
Natural killer cell mediated cytotoxicity (KEGG: hsa04650)
ErbB signaling pathway (KEGG: hsa04012)
Chemokine signaling pathway (KEGG: hsa04062)

Protein Summary

LYN is a 56 kDa Src family tyrosine kinase composed of SH3, SH2, and tyrosine kinase domains. It is anchored to the plasma membrane via N-terminal myristoylation and palmitoylation. LYN phosphorylates immunoreceptor tyrosine-based activation motifs (ITAMs) and inhibitory motifs (ITIMs), modulating signaling from B-cell receptors, Fc receptors, and other immune receptors. It also regulates cytoskeletal reorganization and cell adhesion. Dysregulation of LYN contributes to oncogenesis and autoimmunity.

Related Products

Product name Cat.No. Species Gene ID
LYN Knockout HEK293 Cell Line EDJ-KQ574 Human 4067 Details Get a Quote
LYN Knockout HeLa Cell Line EDJ-KQ18031 Human 4067 Details Get a Quote
LYN Knockout A-549 Cell Line EDJ-KQ18970 Human 4067 Details Get a Quote
LYN Knockout HCT 116 Cell Line EDJ-KQ18971 Human 4067 Details Get a Quote
LYNX1 Knockout HEK293 Cell Line EDJ-KQ51646 Human 66004 Details Get a Quote
LYNX1 Knockout HeLa Cell Line EDJ-KQ57117 Human 66004 Details Get a Quote
LYNX1 Knockout A-549 Cell Line EDJ-KQ65631 Human 66004 Details Get a Quote
LYNX1 Knockout HCT 116 Cell Line EDJ-KQ74054 Human 66004 Details Get a Quote
LYN Knockout HAP1 Cell Line EDC07799 Human 4067 Details Get a Quote
Displaying Records 1 To 9 Of 9 Records
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