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Gene : HCK Homo sapiens

Name  ? HCK proto-oncogene, Src family tyrosine kinase Cytological Location  20q11.21
Brief Description  HCK proto-oncogene, Src family tyrosine kinase
Description  The protein encoded by this gene is a member of the Src family of tyrosine kinases. This protein is primarily hemopoietic, particularly in cells of the myeloid and B-lymphoid lineages. It may help couple the Fc receptor to the activation of the respiratory burst. In addition, it may play a role in neutrophil migration and in the degranulation of neutrophils. Multiple isoforms with different subcellular distributions are produced due to both alternative splicing and the use of alternative translation initiation codons, including a non-AUG (CUG) codon. [provided by RefSeq, Feb 2010]
  • synonyms:
  • OTTHUMG00000032204,
  • AK026432,
  • uc061wdn.1,
  • HGNC:4840,
  • HCK,
  • p59Hck,
  • NM_001172129,
  • hemopoietic cell kinase,
  • JTK9,
  • JTK9,
  • p61Hck
  • identifiers:
  • 3055,
  • ENSG00000101336,
  • HCK

Genome feature

Region: gene ? Length: 49602  
Location: 20:32052242-32101843 Cyto location: 20q11.21

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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]


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Gene Ontology

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118 SN Ps

5 Cross References

18 Data Sets

4 Homologues

1 Located Features

97 Rna Seq Results