thyroid gland disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An endocrine system disease that is located_in the thyroid. (Human Disease Ontology, DOID_50)
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20 genes involed in the disease thyroid gland disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CD40 CD40 molecule, TNF receptor superfamily member 5
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DUOX2 dual oxidase 2
DUOXA2 dual oxidase maturation factor 2
GLIS3 GLIS family zinc finger 3
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IGSF1 immunoglobulin superfamily, member 1
IL2RA interleukin 2 receptor, alpha
IYD iodotyrosine deiodinase
NKX2-1 NK2 homeobox 1
NKX2-5 NK2 homeobox 5
PAX8 paired box 8
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SCGB3A2 secretoglobin, family 3A, member 2
SLC5A5 solute carrier family 5 (sodium/iodide cotransporter), member 5
TG thyroglobulin
THRA thyroid hormone receptor, alpha
TPO thyroid peroxidase
TSHB thyroid stimulating hormone, beta
TSHR thyroid stimulating hormone receptor