hyperthyroidism Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description A thyroid gland disease that involves an over production of thyroid hormone. (Human Disease Ontology, DOID_7998)
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Genes

28 genes co-occuring with the biological term hyperthyroidism in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
CASQ2 calsequestrin 2 (cardiac muscle)
CD40 CD40 molecule, TNF receptor superfamily member 5
CGA glycoprotein hormones, alpha polypeptide
CHGA chromogranin A
CPB2 carboxypeptidase B2 (plasma)
CTLA4 cytotoxic T-lymphocyte-associated protein 4
FCRL3 Fc receptor-like 3
FGF23 fibroblast growth factor 23
GHRL ghrelin/obestatin prepropeptide
IFNG interferon, gamma
IGF1 insulin-like growth factor 1 (somatomedin C)
IGFBP1 insulin-like growth factor binding protein 1
IL18 interleukin 18
IL6 interleukin 6
LMOD1 leiomodin 1 (smooth muscle)
NAMPT nicotinamide phosphoribosyltransferase
NUCB2 nucleobindin 2
RETN resistin
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
TG thyroglobulin
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
TNF tumor necrosis factor
TNFSF13B tumor necrosis factor (ligand) superfamily, member 13b
TSHR thyroid stimulating hormone receptor