Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 Biomarker disease CTD_human
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B. 7693130 1993
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene. 7693129 1993
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT The same MPZ locus cosegregates with the CMT1B disease gene in a second CMT1B family [total multipoint logarithm of odds (lod) = 11.4 at theta = 0.00] with a splice junction mutation. 7504284 1993
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Mutation of the myelin P0 gene in Charcot-Marie-tooth neuropathy type 1. 7688964 1993
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT New mutation of the myelin P0 gene in a pedigree of Charcot-Marie-Tooth neuropathy 1. 7505151 1993
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B. 7694726 1993
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B. 7530774 1994
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 gene. 7527371 1994
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Charcot-Marie-Tooth type 1B neuropathy: third mutation of serine 63 codon in the major peripheral myelin glycoprotein PO gene. 8835320 1995
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B. 7550231 1995
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease. 8797476 1996
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Charcot-Marie-Tooth type 1B neuropathy: a mutation at the single glycosylation site in the major peripheral myelin glycoprotein Po. 8844219 1996
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Mutations in the MPZ gene are associated with the demyelinating peripheral neuropathies Charcot-Marie-Tooth disease type 1B (CMT1B), and the more severe Dejerine-Sottas syndrome (DSS). 8664899 1996
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. 8816708 1996
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Novel mutation of the myelin P0 gene in a CMT1B family. 8990016 1997
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. 9187667 1997
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Novel mutation of the myelin Po gene in a pedigree with Charcot-Marie-Tooth disease type 1B. 9217235 1997
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Mutation analysis in Charcot-Marie-Tooth disease type 1 (CMT1). 9452099 1998
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Spectrum of mutations in Finnish patients with Charcot-Marie-Tooth disease and related neuropathies. 9633821 1998
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Mutations of the same sequence of the myelin P0 gene causing two different phenotypes. 9452091 1998
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths. 10214757 1999
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Peripheral myelin modification in CMT1B correlates with MPZ gene mutations. 10545037 1999
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		1.000 GeneticVariation disease UNIPROT Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients. 10737979 2000