beta-ketothiolase deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14723)
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14 genes co-occuring with the disease beta-ketothiolase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ACAT1 acetyl-CoA acetyltransferase 1 3.23654
ACAT2 acetyl-CoA acetyltransferase 2 2.40982
ACAA2 acetyl-CoA acyltransferase 2 2.15976
ACAA1 acetyl-CoA acyltransferase 1 1.87148
HMGCL 3-hydroxymethyl-3-methylglutaryl-CoA lyase 1.86049
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10 1.37643
CUTA cutA divalent cation tolerance homolog (E. coli) 0.941196
ETFA electron-transfer-flavoprotein, alpha polypeptide 0.901567
GCDH glutaryl-CoA dehydrogenase 0.808949
PC pyruvate carboxylase 0.629635
MUT methylmalonyl CoA mutase 0.564889
PEX6 peroxisomal biogenesis factor 6 0.492359
SCN2A sodium channel, voltage gated, type II alpha subunit 0.452962
PEX2 peroxisomal biogenesis factor 2 0.450701