Gene: CDK2AP1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8099
Gene Symbol: CDK2AP1
CDK2AP1 		0.100 CausalMutation disease CLINVAR Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial Disease. 27858754 2015
Entrez Id: 8099
Gene Symbol: CDK2AP1
CDK2AP1 		0.100 GeneticVariation disease CLINVAR Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial Disease. 27858754 2015
Entrez Id: 8099
Gene Symbol: CDK2AP1
CDK2AP1 		0.100 CausalMutation disease CLINVAR Optic atrophy and a Leigh-like syndrome due to mutations in the c12orf65 gene: report of a novel mutation and review of the literature. 24284555 2014
Entrez Id: 8099
Gene Symbol: CDK2AP1
CDK2AP1 		0.100 GeneticVariation disease CLINVAR Optic atrophy and a Leigh-like syndrome due to mutations in the c12orf65 gene: report of a novel mutation and review of the literature. 24284555 2014
Entrez Id: 8099
Gene Symbol: CDK2AP1
CDK2AP1 		0.100 GeneticVariation disease CLINVAR Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect. 20598281 2010
Entrez Id: 8099
Gene Symbol: CDK2AP1
CDK2AP1 		0.100 CausalMutation disease CLINVAR Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect. 20598281 2010