Hyperoxaluria Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Increased excretion of oxalates in the urine. (Human Phenotype Ontology, HP_0003159)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D006959
Similar Terms
Downloads & Tools

Genes

5 genes/proteins associated with the disease Hyperoxaluria from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 2.88009
CCL2 chemokine (C-C motif) ligand 2 2.88009
CCL5 chemokine (C-C motif) ligand 5 2.88009
SLC26A1 solute carrier family 26 (anion exchanger), member 1 2.88009
IL6 interleukin 6 2.88009