Thyrotoxicosis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A thyroid gland disease that is characterized by excess thyroid hormone. (Human Disease Ontology, DOID_7997)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D013971
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Genes

16 genes/proteins associated with the disease Thyrotoxicosis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MTHFR methylenetetrahydrofolate reductase (NAD(P)H) 2.88009
TSHR thyroid stimulating hormone receptor 2.88009
TSHB thyroid stimulating hormone, beta 1.36247
THRB thyroid hormone receptor, beta 1.32993
SLC5A5 solute carrier family 5 (sodium/iodide cotransporter), member 5 1.20064
GJA5 gap junction protein, alpha 5, 40kDa 1.18226
THRA thyroid hormone receptor, alpha 1.17
CDA cytidine deaminase 1.11431
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) 1.08372
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.08196
GFAP glial fibrillary acidic protein 1.06952
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8) 1.05386
MMP2 matrix metallopeptidase 2 1.04389
DIO1 deiodinase, iodothyronine, type I 1.02634
AMY1A amylase, alpha 1A (salivary) 1.01928
ODC1 ornithine decarboxylase 1 1.01701