Pseudohypoparathyroidism 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_4184)
External Link https://www.disgenet.org/browser/0/1/0/C1864100
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Genes

36 genes associated with the disease Pseudohypoparathyroidism 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
APRT adenine phosphoribosyltransferase
ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1
BRD2 bromodomain containing 2
BRS3 bombesin-like receptor 3
CALCA calcitonin-related polypeptide alpha
COASY CoA synthase
CXCR6 chemokine (C-X-C motif) receptor 6
EDNRA endothelin receptor type A
GH1 growth hormone 1
GHRH growth hormone releasing hormone
GNAS GNAS complex locus
GPR42 G protein-coupled receptor 42 (gene/pseudogene)
HCAR3 hydroxycarboxylic acid receptor 3
LPAR2 lysophosphatidic acid receptor 2
MC4R melanocortin 4 receptor
MFAP1 microfibrillar-associated protein 1
PDE4D phosphodiesterase 4D, cAMP-specific
PDGFB platelet-derived growth factor beta polypeptide
PHPT1 phosphohistidine phosphatase 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRMT7 protein arginine methyltransferase 7
PTH parathyroid hormone
PTH1R parathyroid hormone 1 receptor
PTHLH parathyroid hormone-like hormone
PTRH1 peptidyl-tRNA hydrolase 1 homolog (S. cerevisiae)
REN renin
SNU13 small nuclear ribonucleoprotein 13
SOX3 SRY (sex determining region Y)-box 3
SSTR4 somatostatin receptor 4
STK25 serine/threonine kinase 25
STX16 syntaxin 16
TRH thyrotropin-releasing hormone
WDR20 WD repeat domain 20