Parathyroid Hyperplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hyperplasia of the parathyroid gland. (Human Phenotype Ontology, HP_0008208)
External Link https://www.disgenet.org/browser/0/1/0/C0271844
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Genes

36 genes associated with the disease Parathyroid Hyperplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
ARR3 arrestin 3, retinal (X-arrestin)
CASR calcium-sensing receptor
CCND1 cyclin D1
CDC73 cell division cycle 73
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CDKN1B cyclin-dependent kinase inhibitor 1B (p27, Kip1)
CDKN2B cyclin-dependent kinase inhibitor 2B (p15, inhibits CDK4)
CDKN2C cyclin-dependent kinase inhibitor 2C (p18, inhibits CDK4)
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CHGA chromogranin A
CXADR coxsackie virus and adenovirus receptor
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
EGF epidermal growth factor
EGFR epidermal growth factor receptor
FGF23 fibroblast growth factor 23
KL klotho
LEP leptin
MCAT malonyl CoA:ACP acyltransferase (mitochondrial)
MCPH1 microcephalin 1
MEN1 multiple endocrine neoplasia I
NPS neuropeptide S
NR1I3 nuclear receptor subfamily 1, group I, member 3
PPP2R1B protein phosphatase 2, regulatory subunit A, beta
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
PTH parathyroid hormone
PTHLH parathyroid hormone-like hormone
RET ret proto-oncogene
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TGFA transforming growth factor, alpha
TNFSF10 tumor necrosis factor (ligand) superfamily, member 10
TPO thyroid peroxidase
TRIM13 tripartite motif containing 13
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor