serine deficiency 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 has_material_basis_in defects in the biosynthesis of the amino acid L-serine. (Human Disease Ontology, DOID_0050721)
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12 genes co-occuring with the disease serine deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PHGDH phosphoglycerate dehydrogenase 2.35252
PSPH phosphoserine phosphatase 2.14073
PSAT1 phosphoserine aminotransferase 1 1.73094
SRR serine racemase 1.54805
SUOX sulfite oxidase 1.49174
BCAT1 branched chain amino-acid transaminase 1, cytosolic 1.37556
TALDO1 transaldolase 1 1.05471
ALDH5A1 aldehyde dehydrogenase 5 family, member A1 0.910199
SHMT1 serine hydroxymethyltransferase 1 (soluble) 0.906909
GLUL glutamate-ammonia ligase 0.615529
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 0.412779
SYP synaptophysin 0.223853