histidine metabolism disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that involves deficiency in histidine. (Human Disease Ontology, DOID_9265)
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15 genes co-occuring with the disease histidine metabolism disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HAL histidine ammonia-lyase 3.21145
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1 1.24385
SLC7A5P2 solute carrier family 7 (amino acid transporter light chain, L system), member 5 pseudogene 2 1.17035
ADSL adenylosuccinate lyase 1.10006
KIF21A kinesin family member 21A 0.964148
QDPR quinoid dihydropteridine reductase 0.829869
NT5E 5'-nucleotidase, ecto (CD73) 0.590948
CS citrate synthase 0.51919
TRIM37 tripartite motif containing 37 0.496939
PAH phenylalanine hydroxylase 0.491978
PKLR pyruvate kinase, liver and RBC 0.391141
MMD monocyte to macrophage differentiation-associated 0.374438
CAT catalase 0.329565
PKM pyruvate kinase, muscle 0.32701
SOD2 superoxide dismutase 2, mitochondrial 0.215992