Calcium Pyrophosphate Deposition Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0553730
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Genes

32 genes associated with the disease Calcium Pyrophosphate Deposition Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
ANK1 ankyrin 1, erythrocytic
ANKH ANKH inorganic pyrophosphate transport regulator
ANXA5 annexin A5
AP2S1 adaptor-related protein complex 2, sigma 1 subunit
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATP7B ATPase, Cu++ transporting, beta polypeptide
CDC73 cell division cycle 73
CLCNKB chloride channel, voltage-sensitive Kb
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FXYD2 FXYD domain containing ion transport regulator 2
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GCM2 glial cells missing homolog 2 (Drosophila)
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
HFE hemochromatosis
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
IL17A interleukin 17A
INSRR insulin receptor-related receptor
KCNJ1 potassium channel, inwardly rectifying subfamily J, member 1
KL klotho
LMNA lamin A/C
MEN1 multiple endocrine neoplasia I
MMP3 matrix metallopeptidase 3
NOTCH3 notch 3
PDGFRB platelet-derived growth factor receptor, beta polypeptide
POMC proopiomelanocortin
PTH parathyroid hormone
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
WRN Werner syndrome, RecQ helicase-like