Gene: DNM1L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.110 Biomarker phenotype BEFREE Drp1 deficiency has been associated with one of the major types of ataxia: autosomal recessive spastic ataxia of Charlevoix Saguenay. 28527629 2018
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.110 Biomarker phenotype HPO