JAK2 Chromosome 9

Janus kinase 2
20 variants 20 Health Risk

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What This Gene Does
This gene encodes a non-receptor tyrosine kinase that plays a central role in cytokine and growth factor signalling. The primary isoform of this protein has an N-terminal FERM domain that is required for erythropoietin receptor association, an SH2 domain that binds STAT transcription factors, a pseudokinase domain and a C-terminal tyrosine kinase domain. Cytokine binding induces autophosphorylation and activation of this kinase. This kinase then recruits and phosphorylates signal transducer and activator of transcription (STAT) proteins. Growth factors like TGF-beta 1 also induce phosphorylation and activation of this kinase and translocation of downstream STAT proteins to the nucleus where they influence gene transcription. Mutations in this gene are associated with numerous inflammatory diseases and malignancies. This gene is a downstream target of the pleiotropic cytokine IL6 that is produced by B cells, T cells, dendritic cells and macrophages to produce an immune response or inflammation. Disregulation of the IL6/JAK2/STAT3 signalling pathways produces increased cellular proliferation and myeloproliferative neoplasms of hematopoietic stem cells. A nonsynonymous mutation in the pseudokinase domain of this gene disrupts the domains inhibitory effect and results in constitutive tyrosine phosphorylation activity and hypersensitivity to cytokine signalling. This gene and the IL6/JAK2/STAT3 signalling pathway is a therapeutic target for the treatment of excessive inflammatory responses to viral infections. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2020]
Gene Info
Gene Group
"SH2 domain containing|FERM domain containing|Jak family tyrosine kinases"
Locus Type
gene with protein product
Location
9p24.1
Ensembl
ENSG00000096968
Associated Conditions (19)
Premature ovarian failure
Inborn genetic diseases
Hereditary cancer
Acquired polycythemia vera
Primary myelofibrosis
Budd-Chiari syndrome
Thrombocythemia 3
6 conditions
Inherited susceptibility to asthma
JAK2-related disorder
See cases
Hepatocellular carcinoma
Acute myeloid leukemia
susceptibility to
somatic
Primary familial polycythemia due to EPO receptor mutation
Myeloproliferative disorder
Polycythemia
Splenomegaly
Key Variants
All Variants (20)
RSID Category Clinical Significance Conditions
RS1299892808 Health Risk Conflicting classifications of pathogenicity Premature ovarian failure, Premature ovarian failure
RS138655335 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS139504737 Health Risk Conflicting classifications of pathogenicity Hereditary cancer, Acquired polycythemia vera, Primary myelofibrosis
RS142269166 Health Risk Conflicting classifications of pathogenicity Thrombocythemia 3, Thrombocythemia 3
RS1426814242 Health Risk Conflicting classifications of pathogenicity
RS143103233 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS143227399 Health Risk Conflicting classifications of pathogenicity
RS150159583 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS150221602 Health Risk Conflicting classifications of pathogenicity Inherited susceptibility to asthma, Inherited susceptibility to asthma
RS182123615 Health Risk Conflicting classifications of pathogenicity Acquired polycythemia vera, 6 conditions, JAK2-related disorder
RS2230723 Health Risk Conflicting classifications of pathogenicity
RS368927897 Health Risk Conflicting classifications of pathogenicity
RS372254348 Health Risk Conflicting classifications of pathogenicity JAK2-related disorder, 6 conditions, JAK2-related disorder
RS529050943 Health Risk Conflicting classifications of pathogenicity 6 conditions, 6 conditions
RS533264615 Health Risk Conflicting classifications of pathogenicity
RS892216772 Health Risk Conflicting classifications of pathogenicity Thrombocythemia 3, Thrombocythemia 3
RS1486560342 Health Risk Likely pathogenic
RS2488857097 Health Risk Likely pathogenic See cases, Hepatocellular carcinoma, See cases
RS121912472 Health Risk Pathogenic Acute myeloid leukemia, Acute myeloid leukemia
RS77375493 Health Risk Pathogenic Acquired polycythemia vera, Primary myelofibrosis, Acute myeloid leukemia
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