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 		0.110 GeneticVariation disease BEFREE We found the association of a heterozygous novel MPZ gene point mutation, Ile62Phe in exon 2, with autosomal dominant motor and sensory neuropathy with focally folded myelin sheaths. 10214757 1999
Entrez Id: 4359
Gene Symbol: MPZ
MPZ 		0.110 GeneticVariation disease CLINVAR