ornithine translocase 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 deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood. (Human Disease Ontology, DOID_0050720)
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Genes

12 genes co-occuring with the disease ornithine translocase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SLC25A15 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 3.17876
SLC25A2 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 2 2.11194
SLC25A29 solute carrier family 25 (mitochondrial carnitine/acylcarnitine carrier), member 29 1.72228
ACO2 aconitase 2, mitochondrial 1.3712
OTC ornithine carbamoyltransferase 1.12909
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8 1.09755
OGDH oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide) 0.795002
LIG3 ligase III, DNA, ATP-dependent 0.699517
OAT ornithine aminotransferase 0.594064
DNAH8 dynein, axonemal, heavy chain 8 0.461261
GPX5 glutathione peroxidase 5 0.162306
GPX4 glutathione peroxidase 4 0.160761