Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 Biomarker RGD Evaluation of bone marrow reticulin formation in chronic immune thrombocytopenia patients treated with romiplostim. 19671919

2009

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation BEFREE These data indicate that MPL mutation in myelofibrosis characterises patients with more severe anaemic phenotype. 17408465

2007

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation BEFREE Evidence for MPL W515L/K mutations in hematopoietic stem cells in primitive myelofibrosis. 17709604

2007

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation UNIPROT DNA sequence analysis of the exons encoding the transmembrane and juxtamembrane domains of EPOR, MPL, and GCSFR, and comparison with germline DNA derived from buccal swabs, identified a somatic activating mutation in the transmembrane domain of MPL (W515L) in 9% (4/45) of JAKV617F-negative MF. 16834459

2006

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 SomaticCausalMutation ORPHANET The diagnosis of patients with mutant MPL alleles at the time of molecular testing was de novo MMM in 12 patients, ET in 4, post-ET MMM in 1, and MMM in blast crisis in 3. 16868251

2006

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 SomaticCausalMutation ORPHANET DNA sequence analysis of the exons encoding the transmembrane and juxtamembrane domains of EPOR, MPL, and GCSFR, and comparison with germline DNA derived from buccal swabs, identified a somatic activating mutation in the transmembrane domain of MPL (W515L) in 9% (4/45) of JAKV617F-negative MF. 16834459

2006

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation UNIPROT The diagnosis of patients with mutant MPL alleles at the time of molecular testing was de novo MMM in 12 patients, ET in 4, post-ET MMM in 1, and MMM in blast crisis in 3. 16868251

2006

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation BEFREE DNA sequence analysis of the exons encoding the transmembrane and juxtamembrane domains of EPOR, MPL, and GCSFR, and comparison with germline DNA derived from buccal swabs, identified a somatic activating mutation in the transmembrane domain of MPL (W515L) in 9% (4/45) of JAKV617F-negative MF. 16834459

2006

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 GeneticVariation BEFREE The diagnosis of patients with mutant MPL alleles at the time of molecular testing was de novo MMM in 12 patients, ET in 4, post-ET MMM in 1, and MMM in blast crisis in 3. 16868251

2006

Entrez Id: 4352
Gene Symbol: MPL
MPL
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis
0.900 CausalMutation CLINVAR