Gene Gene information from NCBI Gene database.
Entrez ID 4067
Gene name LYN proto-oncogene, Src family tyrosine kinase
Gene symbol LYN
Synonyms (NCBI Gene)
JTK8SAIDVp53Lynp56Lyn
Chromosome 8
Chromosome location 8q12.1
Summary This gene encodes a tyrosine protein kinase, which maybe involved in the regulation of mast cell degranulation, and erythroid differentiation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided b
miRNA miRNA information provided by mirtarbase database.
117
miRTarBase ID miRNA Experiments Reference
MIRT046575 hsa-miR-222-3p CLASH 23622248
MIRT322915 hsa-miR-32-3p PAR-CLIP 20371350
MIRT322916 hsa-miR-4731-3p PAR-CLIP 20371350
MIRT322917 hsa-miR-4801 PAR-CLIP 20371350
MIRT570814 hsa-miR-4789-3p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
205
GO ID Ontology Definition Evidence Reference
GO:0000077 Process DNA damage checkpoint signaling IDA 10891478
GO:0000166 Function Nucleotide binding IEA
GO:0000902 Process Cell morphogenesis IEA
GO:0001782 Process B cell homeostasis IEA
GO:0001782 Process B cell homeostasis ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
165120 6735 ENSG00000254087
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P07948
Protein name Tyrosine-protein kinase Lyn (EC 2.7.10.2) (Lck/Yes-related novel protein tyrosine kinase) (V-yes-1 Yamaguchi sarcoma viral related oncogene homolog) (p53Lyn) (p56Lyn)
Protein function Non-receptor tyrosine-protein kinase that transmits signals from cell surface receptors and plays an important role in the regulation of innate and adaptive immune responses, hematopoiesis, responses to growth factors and cytokines, integrin sig
PDB 1W1F , 1WA7 , 3A4O , 5XY1 , 6NMW , 8WFF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00018 SH3_1 69 115 SH3 domain Domain
PF00017 SH2 129 211 SH2 domain Domain
PF07714 PK_Tyr_Ser-Thr 247 497 Protein tyrosine and serine/threonine kinase Domain
Tissue specificity TISSUE SPECIFICITY: Detected in monocytes (at protein level). Detected in placenta, and in fetal brain, lung, liver and kidney. Widely expressed in a variety of organs, tissues, and cell types such as epidermoid, hematopoietic, and neuronal cells. Express
Sequence
Sequence length 512
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Chemokine signaling pathway
NF-kappa B signaling pathway
Platelet activation
B cell receptor signaling pathway
Fc epsilon RI signaling pathway
Fc gamma R-mediated phagocytosis
Long-term depression
Epithelial cell signaling in Helicobacter pylori infection
Kaposi sarcoma-associated herpesvirus infection
Epstein-Barr virus infection
Viral carcinogenesis
Lipid and atherosclerosis
  GPVI-mediated activation cascade
Signaling by SCF-KIT
Regulation of KIT signaling
Cell surface interactions at the vascular wall
FCGR activation
PECAM1 interactions
Fc epsilon receptor (FCERI) signaling
Role of LAT2/NTAL/LAB on calcium mobilization
FCERI mediated MAPK activation
FCERI mediated Ca+2 mobilization
FCERI mediated NF-kB activation
CD28 co-stimulation
CTLA4 inhibitory signaling
EPHB-mediated forward signaling
EPHA-mediated growth cone collapse
EPH-ephrin mediated repulsion of cells
Dectin-2 family
CD209 (DC-SIGN) signaling
CD22 mediated BCR regulation
Cyclin D associated events in G1
Platelet Adhesion to exposed collagen
Erythropoietin activates Phosphoinositide-3-kinase (PI3K)
Erythropoietin activates RAS
Regulation of signaling by CBL
FCGR3A-mediated IL10 synthesis
FCGR3A-mediated phagocytosis
Growth hormone receptor signaling
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
12
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autoinflammatory disease, systemic, with vasculitis Pathogenic rs2486900565, rs1585690632, rs2486900588, rs2486900574 RCV003228812
RCV003228884
RCV003228813
RCV003228743
LYN kinase associated vasculopathy and liver fibrosis syndrome Pathogenic rs2486900565, rs1585690632, rs2486900588 RCV002512493
RCV002512494
RCV002512495
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
LYN-related disorder Benign; Likely benign; Uncertain significance rs142291090, rs867077413, rs763145713 RCV003908864
RCV003408024
RCV004756338
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 26708841, 27756880, 36991000
Adenocarcinoma of Lung Associate 23866081, 27756880
Anovulation Associate 40287692
Atherosclerosis Associate 28260035, 34122426
Autoimmune Diseases Associate 36215934, 36267464
Bone Resorption Associate 9844106
Brain Ischemia Associate 33460396
Breast Neoplasms Associate 20215510, 30969999
Bruton type agammaglobulinemia Associate 10688822
Burkitt Lymphoma Associate 26731115