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 		0.410 GeneticVariation disease BEFREE Postnatal microcephaly and pain insensitivity due to a de novo heterozygous DNM1L mutation causing impaired mitochondrial fission and function. 26992161 2016
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.410 Biomarker disease CTD_human A lethal defect of mitochondrial and peroxisomal fission. 17460227 2007
Entrez Id: 10059
Gene Symbol: DNM1L
DNM1L 		0.410 Biomarker disease HPO