Histidinemia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A histidine metabolism disease that involves a deficiency of the enzyme histidase. (Human Disease Ontology, DOID_0060168)
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Genes

59 genes co-occuring with the disease Histidinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
HAL histidine ammonia-lyase 3.25
ADSL adenylosuccinate lyase 2.542
METTL22 methyltransferase like 22 2.206
GOT1L1 glutamic-oxaloacetic transaminase 1-like 1 2.016
UROC1 urocanate hydratase 1 1.999
NIT2 nitrilase family, member 2 1.932
HAO2 hydroxyacid oxidase 2 (long chain) 1.874
HYKK hydroxylysine kinase 1.852
QDPR quinoid dihydropteridine reductase 1.848
NANS N-acetylneuraminic acid synthase 1.768
KIN Kin17 DNA and RNA binding protein 1.748
SLC5A10 solute carrier family 5 (sodium/sugar cotransporter), member 10 1.742
GLDC glycine dehydrogenase (decarboxylating) 1.724
UPB1 ureidopropionase, beta 1.69
AMT aminomethyltransferase 1.671
AP2A1 adaptor-related protein complex 2, alpha 1 subunit 1.662
PTER phosphotriesterase related 1.656
OR2T11 olfactory receptor, family 2, subfamily T, member 11 (gene/pseudogene) 1.637
LRSAM1 leucine rich repeat and sterile alpha motif containing 1 1.621
PCBD1 pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha 1.572
FTCD formimidoyltransferase cyclodeaminase 1.532
AHCY adenosylhomocysteinase 1.531
PHYKPL 5-phosphohydroxy-L-lysine phospho-lyase 1.528
ASPA aspartoacylase 1.492
BCKDHB branched chain keto acid dehydrogenase E1, beta polypeptide 1.471
GOT1 glutamic-oxaloacetic transaminase 1, soluble 1.452
DPYD dihydropyrimidine dehydrogenase 1.433
GCSH glycine cleavage system protein H (aminomethyl carrier) 1.431
MAT1A methionine adenosyltransferase I, alpha 1.431
PRODH proline dehydrogenase (oxidase) 1 1.398
SLC7A9 solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9 1.367
DMGDH dimethylglycine dehydrogenase 1.365
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 1.349
GDPD4 glycerophosphodiester phosphodiesterase domain containing 4 1.342
RBM26 RNA binding motif protein 26 1.32
TCEAL9 transcription elongation factor A like 9 1.306
ETFDH electron-transferring-flavoprotein dehydrogenase 1.293
PPEF2 protein phosphatase, EF-hand calcium binding domain 2 1.293
BCAT2 branched chain amino-acid transaminase 2, mitochondrial 1.273
IPMK inositol polyphosphate multikinase 1.237
OAT ornithine aminotransferase 1.219
BCKDHA branched chain keto acid dehydrogenase E1, alpha polypeptide 1.214
ALDH1L1 aldehyde dehydrogenase 1 family, member L1 1.197
AMDHD1 amidohydrolase domain containing 1 1.178
SLC3A1 solute carrier family 3 (amino acid transporter heavy chain), member 1 1.171
ATP6V1G3 ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G3 1.152
KIF16B kinesin family member 16B 1.136
DIS3L DIS3 like exosome 3'-5' exoribonuclease 1.133
LTA4H leukotriene A4 hydrolase 1.132
ATP6V0E1 ATPase, H+ transporting, lysosomal 9kDa, V0 subunit e1 1.116
FBXO40 F-box protein 40 1.091
STXBP5L syntaxin binding protein 5-like 1.066
ATP6V1F ATPase, H+ transporting, lysosomal 14kDa, V1 subunit F 1.066
ETNPPL ethanolamine-phosphate phospho-lyase 1.048
LRRN1 leucine rich repeat neuronal 1 1.035
MATK megakaryocyte-associated tyrosine kinase 1.031
ACADS acyl-CoA dehydrogenase, C-2 to C-3 short chain 1.03
SLCO5A1 solute carrier organic anion transporter family, member 5A1 1.025
KYAT3 kynurenine aminotransferase 3 1.012