COQ2, coenzyme Q2, polyprenyltransferase, 27235

N. diseases: 139; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 Biomarker disease GENOMICS_ENGLAND [Clinical analysis of one infantile nephrotic syndrome caused by COQ2 gene mutation and literature review]. 30180404 2018
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease UNIPROT Further phenotypic heterogeneity of CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 and COQ6 variants. 28044327 2017
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 CausalMutation disease CLINVAR The COQ2 genotype predicts the severity of coenzyme Q10 deficiency. 27493029 2016
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease UNIPROT The COQ2 genotype predicts the severity of coenzyme Q10 deficiency. 27493029 2016
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 CausalMutation disease CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159 2015
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease UNIPROT Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure. 25564041 2015
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 Biomarker disease GENOMICS_ENGLAND A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies. 25655951 2015
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 Biomarker disease GENOMICS_ENGLAND Genome sequencing identifies major causes of severe intellectual disability. 24896178 2014
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease UNIPROT A novel mutation in COQ2 leading to fatal infantile multisystem disease. 23343605 2013
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease UNIPROT Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis. 17374725 2007
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 CausalMutation disease CLINVAR COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement. 17855635 2007
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease UNIPROT COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement. 17855635 2007
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 Biomarker disease GENOMICS_ENGLAND Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders. 17332895 2007
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease UNIPROT A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency. 16400613 2006
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 Biomarker disease CTD_human
CUI: C3551954
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 1
COENZYME Q10 DEFICIENCY, PRIMARY, 1 		0.700 GeneticVariation disease CLINVAR
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		0.600 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		0.600 Biomarker disease GENOMICS_ENGLAND Genome sequencing identifies major causes of severe intellectual disability. 24896178 2014
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations in COQ2 in familial and sporadic multiple-system atrophy. 23758206 2013
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		0.600 GeneticVariation disease UNIPROT Mutations in COQ2 in familial and sporadic multiple-system atrophy. 23758206 2013
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		0.600 Biomarker disease GENOMICS_ENGLAND Multiplex families with multiple system atrophy. 17420317 2007
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		0.600 SusceptibilityMutation disease CLINVAR
CUI: C1843920
Disease: COENZYME Q10 DEFICIENCY
COENZYME Q10 DEFICIENCY 		0.380 GeneticVariation disease BEFREE COQ2 gene mutations not only cause primary coenzyme Q10 deficiency but also cause SRNS without extrarenal manifestations. 31660881 2019
CUI: C1843920
Disease: COENZYME Q10 DEFICIENCY
COENZYME Q10 DEFICIENCY 		0.380 GeneticVariation disease BEFREE The COQ2 genotype predicts the severity of coenzyme Q10 deficiency. 27493029 2016