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Gene JAK2
Variant T875N
Impact List missense
Protein Effect gain of function
Gene Variant Descriptions JAK2 T875N lies within the protein kinase domain 2 of the Jak2 protein (UniProt.org). T875N confers a gain of function to the Jak2 protein as demonstrated by increased Jak2 and Stat1, Stat3, and Stat5 phosphorylation (PMID: 19543316), and is transforming in cell culture (PMID: 21362419, PMID: 31299252).
Associated Drug Resistance
Category Variants Paths

JAK2 mutant JAK2 act mut JAK2 T875N

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Transcript NM_004972.4
gDNA chr9:g.5089726C>A
cDNA c.2624C>A
Protein p.T875N
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001322195.2 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322194 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322194.2 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322195 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322196 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_004972.4 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_004972.3 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322196.2 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322195.1 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322194.1 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_004972 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38
NM_001322196.1 chr9:g.5089726C>A c.2624C>A p.T875N RefSeq GRCh38/hg38

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
JAK2 mutant B-cell acute lymphoblastic leukemia not applicable N/A Guideline Prognostic JAK2 mutations are associated with a poor prognosis in patients with B-cell acute lymphoblastic leukemia (NCCN.org). detail...
JAK2 mutant essential thrombocythemia not applicable N/A Guideline Diagnostic JAK2 mutations aid in the diagnosis of essential thrombocythemia (NCCN.org). detail...
JAK2 mutant childhood B-cell acute lymphoblastic leukemia not applicable N/A Guideline Prognostic JAK2 mutations are associated with a poor prognosis in pediatric patients with B-cell acute lymphoblastic leukemia (NCCN.org). detail...
JAK2 mutant myelofibrosis not applicable N/A Guideline Diagnostic JAK2 mutations aid in the diagnosis of primary myelofibrosis (NCCN.org). detail...