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 		0.700 GeneticVariation disease UNIPROT Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission. 28969390 2017
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.700 CausalMutation disease CLINVAR A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathy. 27145208 2016
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.700 Biomarker disease GENOMICS_ENGLAND A lethal defect of mitochondrial and peroxisomal fission. 17460227 2007
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.700 Biomarker disease CTD_human