graves' disease Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located_in thyroid gland. (Human Disease Ontology, DOID_12361)
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18 genes associated with the disease graves' disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CD40 CD40 molecule, TNF receptor superfamily member 5
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CXCL8 chemokine (C-X-C motif) ligand 8
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
ICAM1 intercellular adhesion molecule 1
IFNG interferon, gamma
IL13 interleukin 13
IL4 interleukin 4
IRF1 interferon regulatory factor 1
LTA lymphotoxin alpha
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SCGB3A2 secretoglobin, family 3A, member 2
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
TNF tumor necrosis factor
TSHR thyroid stimulating hormone receptor