mineral metabolism disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An acquired metabolic disease that is characterized by abnormal mineral metabolism. (Human Disease Ontology, DOID_0050032)
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Genes

7 genes involed in the disease mineral metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CLCN5 chloride channel, voltage-sensitive 5
CP ceruloplasmin (ferroxidase)
DMP1 dentin matrix acidic phosphoprotein 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FGF23 fibroblast growth factor 23
PHEX phosphate regulating endopeptidase homolog, X-linked
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3