Gene: DNM2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.020 GeneticVariation disease BEFREE Mutations in dynamin 2 (DNM2), an ubiquitously-expressed large GTPase, cause autosomal dominant centronuclear myopathy (DNM2-CNM) and AD Charcot-Marie-Tooth disease type 2B (DNM2-CMT2B). 17825552 2007
Entrez Id: 1785
Gene Symbol: DNM2
DNM2 		0.020 Biomarker disease BEFREE These features overlap with findings seen in the phenotype of DNM2-related autosomal dominant Charcot-Marie-Tooth disease type 2B. 16585051 2006