Graves Disease Gene Set

Dataset CTD 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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12 genes/proteins associated with the disease Graves Disease from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GRD2 Graves disease, susceptibility to, 2 2.88009
B3GNT2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 2.88009
ARID5B AT rich interactive domain 5B (MRF1-like) 2.88009
TSHR thyroid stimulating hormone receptor 2.88009
IFIH1 interferon induced with helicase C domain 1 2.88009
CTLA4 cytotoxic T-lymphocyte-associated protein 4 2.88009
RNASET2 ribonuclease T2 2.88009
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) 2.88009
FCRL3 Fc receptor-like 3 2.88009
GRDX Graves disease, susceptibility to, X-linked 2.88009
GRD1 Graves disease, susceptiblity to, 1 2.88009
GC group-specific component (vitamin D binding protein) 2.88009