JAK2, Janus kinase 2, 3717

N. diseases: 644; N. variants: 54
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002871
Disease: Anemia
Anemia
0.200 Biomarker disease BEFREE The JAK2-selective inhibitor fedratinib has recently been resurrected, and there has been a resurgence of interest in the failed JAK1/2 inhibitor momelotinib, which possibly improves anemia. 30675650 2019
CUI: C0002871
Disease: Anemia
Anemia
0.200 Biomarker disease BEFREE Combined Janus kinase 1 (JAK1) and JAK2 inhibition therapy effectively reduces splenomegaly and symptom burden related to myelofibrosis but is associated with dose-dependent anemia and thrombocytopenia. 27789678 2017
CUI: C0002871
Disease: Anemia
Anemia
0.200 Biomarker disease BEFREE Anemia is a significant problem and adverse prognostic factor in over a third of MF patients and is often worsened by JAK2 inhibitors. 27785927 2017
CUI: C0002871
Disease: Anemia
Anemia
0.200 Biomarker disease BEFREE Early side effects seen with other less selective JAK inhibitors were not observed (e.g., there was no worsening of anemia [JAK-2 inhibition related], no effects on liver transaminases, and no increase in low-density lipoprotein or total cholesterol). 28622463 2017
CUI: C0002871
Disease: Anemia
Anemia
0.200 Biomarker disease BEFREE Furthermore WT1 is a good marker of response to JAK2 inhibitors especially for patients without blasts and for patients who develop anemia or thrombocytopenia not for progression but as therapy related toxicity. 27167495 2016
CUI: C0002871
Disease: Anemia
Anemia
0.200 GeneticVariation disease BEFREE In primary myelofibrosis patients, the degree of anemia was less severe in those who were CALR exon 9 mutation-positive than in those who were JAK2 V617F-positive (p = 0.048). 25323779 2015
CUI: C0002871
Disease: Anemia
Anemia
0.200 GeneticVariation disease BEFREE However, they often accentuate the anemia and do not reduce the JAK2 allele burden, therefore lacking the potential to modify the natural history of MF. 23514013 2013
CUI: C0002871
Disease: Anemia
Anemia
0.200 AlteredExpression disease BEFREE It is possible that an optimal balance between JAK-1-inhibitory and JAK-2-inhibitory activities may broaden the therapeutic activity (i.e. anemia improvement), as has been preliminarily seen (CYT387). 21245760 2011
CUI: C0002871
Disease: Anemia
Anemia
0.200 GeneticVariation disease BEFREE Median mutation levels in pretreatment ET samples were significantly higher for MPL-mutated cases (60%) than for JAK2-mutated cases (24%; P=0.01), as was presentation with anemia. 20113830 2010
CUI: C0002871
Disease: Anemia
Anemia
0.200 Biomarker disease BEFREE New medical therapies for MF revolve around three main themes: immunomodulation (to assist anemia), hypomethylation strategies, and (the most robust pipeline) the use of targeted JAK2 inhibitors. 20425392 2010
CUI: C0002871
Disease: Anemia
Anemia
0.200 GeneticVariation disease BEFREE In patients with CMD, the multivariate generalized linear regression model showed that the JAK2 (V617F) mutational burden (P = 0.01), serum lactate dehydrogenase level (P = 0.003), and anaemia (P < 0.001) independently correlated with MVD. 18028479 2008
CUI: C0002871
Disease: Anemia
Anemia
0.200 GeneticVariation disease BEFREE When compared with MPL wild-type patients, irrespective of JAK2(V617F) status, those with MPL(W515L/K), were more frequently female, were older (61 years vs. 57 years; P = 0.02), presented with more severe anaemia (haemoglobin, 101 g/l vs. 121 g/l; P = 0.002) and were more likely to require regular transfusional support (P = 0.012). 17408465 2007
CUI: C0002871
Disease: Anemia
Anemia
0.200 GeneticVariation disease BEFREE Apoptotic resistance in MMM correlated with anemia (P=0.01) and the JAK2-V617F (P=0.01). 16871275 2006
CUI: C0002871
Disease: Anemia
Anemia
0.200 Biomarker disease HPO