PRX, periaxin, 57716

N. diseases: 75; N. variants: 21
Disease: Dejerine-Sottas Disease (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10425452
rs10425452
Entrez Id: 57716
Gene Symbol: PRX
PRX
CUI: C0011195
Disease:
Dejerine-Sottas Disease (disorder) 		0.010 GeneticVariation BEFREE In 3 SAMP strains (SAMP3, SAMP10, and SAMP11), we identified a p.R167C missense mutation in the Prx gene, in which mutations causing hereditary motor and sensory neuropathy (Dejerine-Sottas syndrome) have been identified. 23586671 2013