Familial Benign Hypercalcemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1809471
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Genes

23 genes associated with the disease Familial Benign Hypercalcemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACKR3 atypical chemokine receptor 3
ADRA1A adrenoceptor alpha 1A
ADRA2B adrenoceptor alpha 2B
AP2S1 adaptor-related protein complex 2, sigma 1 subunit
ATP2B1 ATPase, Ca++ transporting, plasma membrane 1
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
ATP2B3 ATPase, Ca++ transporting, plasma membrane 3
BCL2 B-cell CLL/lymphoma 2
BRS3 bombesin-like receptor 3
CALCA calcitonin-related polypeptide alpha
CASR calcium-sensing receptor
CD59 CD59 molecule, complement regulatory protein
CDC73 cell division cycle 73
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CXCR6 chemokine (C-X-C motif) receptor 6
EDNRA endothelin receptor type A
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
GPR42 G protein-coupled receptor 42 (gene/pseudogene)
LPAR2 lysophosphatidic acid receptor 2
MEN1 multiple endocrine neoplasia I
PTH parathyroid hormone
RNASE1 ribonuclease, RNase A family, 1 (pancreatic)
SSTR4 somatostatin receptor 4