Gene: MPZ ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 Biomarker disease MGD A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function. 30239779 2019
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 Biomarker disease MGD MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B. 22689911 2012
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 Biomarker disease MGD Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy. 18326085 2008
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 GermlineCausalMutation disease ORPHANET The Roussy-Lévy family: from the original description to the gene. 10553995 1999
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 GeneticVariation disease UNIPROT The Roussy-Lévy family: from the original description to the gene. 10553995 1999
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 Biomarker disease MGD Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies. 7581451 1995
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 Biomarker disease MGD Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons. 1384988 1992
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 CausalMutation disease CLINVAR
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 GeneticVariation disease CLINVAR
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.900 Biomarker disease CTD_human