Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 GeneticVariation disease BEFREE Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. 30740739 2019
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 CausalMutation disease CLINVAR A New Approach for Fast Metabolic Diagnostics in CMAMMA. 26915364 2016
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 Biomarker disease GENOMICS_ENGLAND Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. 27604308 2016
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 CausalMutation disease CLINVAR Added value of next generation gene panel analysis for patients with elevated methylmalonic acid and no clinical diagnosis following functional studies of vitamin B12 metabolism. 26827111 2016
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 GeneticVariation disease CLINVAR Added value of next generation gene panel analysis for patients with elevated methylmalonic acid and no clinical diagnosis following functional studies of vitamin B12 metabolism. 26827111 2016
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 GermlineCausalMutation disease ORPHANET ACSF3 mutant alleles occur with a minor allele frequency of 0.0058 in ∼1,000 control individuals, predicting a CMAMMA population incidence of ∼1:30,000. 21841779 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 GeneticVariation disease CLINVAR ACSF3 mutant alleles occur with a minor allele frequency of 0.0058 in ∼1,000 control individuals, predicting a CMAMMA population incidence of ∼1:30,000. 21841779 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 Biomarker disease BEFREE These results suggest that ACSF3 is a candidate gene for non-classical CMAMMA observed in our patients and document the value of exome sequencing of a limited number of patients for the identification of novel disease genes. 21785126 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 Biomarker disease GENOMICS_ENGLAND Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype. 21785126 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 CausalMutation disease CLINVAR Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype. 21785126 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 CausalMutation disease CLINVAR ACSF3 mutant alleles occur with a minor allele frequency of 0.0058 in ∼1,000 control individuals, predicting a CMAMMA population incidence of ∼1:30,000. 21841779 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 GeneticVariation disease BEFREE ACSF3 mutant alleles occur with a minor allele frequency of 0.0058 in ∼1,000 control individuals, predicting a CMAMMA population incidence of ∼1:30,000. 21841779 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 GeneticVariation disease UNIPROT ACSF3 mutant alleles occur with a minor allele frequency of 0.0058 in ∼1,000 control individuals, predicting a CMAMMA population incidence of ∼1:30,000. 21841779 2011
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 197322
Gene Symbol: ACSF3
ACSF3
0.730 Biomarker disease CTD_human