Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 GeneticVariation disease UNIPROT Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathies. 25959673 2015
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 GeneticVariation disease UNIPROT Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing. 25525168 2014
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 GeneticVariation disease UNIPROT Mutations in SCO2 are associated with autosomal-dominant high-grade myopia. 23643385 2013
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 Biomarker disease CTD_human
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 CausalMutation disease CLINVAR
Entrez Id: 9997
Gene Symbol: SCO2
SCO2 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 29781
Gene Symbol: NCAPH2
NCAPH2 		0.100 CausalMutation disease CLINVAR
Entrez Id: 4218
Gene Symbol: RAB8A
RAB8A 		0.010 GeneticVariation disease BEFREE One hundred and thirty-eight high myopic eyes (138 patients) (myopia -6 D or more) were examined more than 12 months after LASEK or Epi-LASIK with advanced surface ablation on the MEL 80 excimer laser (Zeiss AG, Jena, Germany). 29866738 2018