Primary Hyperoxaluria Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2977)
External Link https://www.disgenet.org/browser/0/1/0/C0020501
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Genes

16 genes associated with the disease Primary Hyperoxaluria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGXT alanine-glyoxylate aminotransferase
APRT adenine phosphoribosyltransferase
CRYL1 crystallin, lambda 1
GLUD1 glutamate dehydrogenase 1
GRHPR glyoxylate reductase/hydroxypyruvate reductase
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
HAO1 hydroxyacid oxidase (glycolate oxidase) 1
HAO2 hydroxyacid oxidase 2 (long chain)
HOGA1 4-hydroxy-2-oxoglutarate aldolase 1
KYAT3 kynurenine aminotransferase 3
PRODH2 proline dehydrogenase (oxidase) 2
PTS 6-pyruvoyltetrahydropterin synthase
RBMXL1 RNA binding motif protein, X-linked-like 1
SULT1E1 sulfotransferase family 1E, estrogen-preferring, member 1
UGDH UDP-glucose 6-dehydrogenase