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Gene : FYN Homo sapiens

Name  ? FYN proto-oncogene, Src family tyrosine kinase Cytological Location  6q21
Brief Description  FYN proto-oncogene, Src family tyrosine kinase
Description  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 interacts with the fyn-binding protein. Alternatively spliced transcript variants encoding distinct isoforms exist. [provided by RefSeq, Jul 2008]
  • synonyms:
  • SYN,
  • uc003pvk.3,
  • SLK,
  • FYN,
  • SYN,
  • HGNC:4037,
  • MGC45350,
  • OTTHUMG00000016305,
  • p59-FYN,
  • NM_001370529,
  • AK056699,
  • SLK,
  • FYN oncogene related to SRC, FGR, YES
  • identifiers:
  • 2534,
  • ENSG00000010810,
  • FYN

Genome feature

Region: gene ? Length: 213121  
Location: 6:111660332-111873452 reverse strand Cyto location: 6q21


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Function

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87 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Expression

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Other

87 Pathways

811 SN Ps

5 Cross References

18 Data Sets

4 Homologues

3 Located Features

97 Rna Seq Results