C-Cell Hyperplasia Of Thyroid Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0342190
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Genes

33 genes associated with the disease C-Cell Hyperplasia Of Thyroid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AOC1 amine oxidase, copper containing 1
AR androgen receptor
ATF4 activating transcription factor 4
BDNF brain-derived neurotrophic factor
BRAF B-Raf proto-oncogene, serine/threonine kinase
CALCA calcitonin-related polypeptide alpha
CCDC6 coiled-coil domain containing 6
CCKBR cholecystokinin B receptor
DDC dopa decarboxylase (aromatic L-amino acid decarboxylase)
DPP4 dipeptidyl-peptidase 4
EGFR epidermal growth factor receptor
F9 coagulation factor IX
GLP1R glucagon-like peptide 1 receptor
INSL3 insulin-like 3 (Leydig cell)
MT1A metallothionein 1A
NKX2-1 NK2 homeobox 1
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PTCH1 patched 1
PTEN phosphatase and tensin homolog
PTH parathyroid hormone
PTTG1 pituitary tumor-transforming 1
RET ret proto-oncogene
RXFP1 relaxin/insulin-like family peptide receptor 1
RXFP2 relaxin/insulin-like family peptide receptor 2
SPP1 secreted phosphoprotein 1
SPRY1 sprouty homolog 1, antagonist of FGF signaling (Drosophila)
TAS2R38 taste receptor, type 2, member 38
TFF1 trefoil factor 1
TGM2 transglutaminase 2
TNC tenascin C
TP53 tumor protein p53
TSHR thyroid stimulating hormone receptor
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase