galactokinase deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A galactosemia that involves an accumulation of galactose and galactitol secondary to the decreased conversion of galactose to galactose-1-phosphate by galactokinase. (Human Disease Ontology, DOID_14695)
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13 genes co-occuring with the disease galactokinase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GALK1 galactokinase 1 3.00494
GALT galactose-1-phosphate uridylyltransferase 1.92576
LGALS1 lectin, galactoside-binding, soluble, 1 1.51545
GALK2 galactokinase 2 1.44782
GALE UDP-galactose-4-epimerase 0.90732
MVK mevalonate kinase 0.706754
SORD sorbitol dehydrogenase 0.661197
MGMT O-6-methylguanine-DNA methyltransferase 0.495411
SP1 Sp1 transcription factor 0.448817
CYGB cytoglobin 0.404184
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8 0.38111
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 0.263014
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase) 0.175947