increased circulating triiodothyronine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater amount of a thyroid hormone present in the blood that regulates growth and development, controls some metabolic processes and body temperature, and negatively regulates secretion of thyrotropin by the pituitary gland (Mammalian Phenotype Ontology, MP_0005480)
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10 gene mutations causing the increased circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGRP agouti related neuropeptide
CPE carboxypeptidase E
DIO1 deiodinase, iodothyronine, type I
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial)
NCOA1 nuclear receptor coactivator 1
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
VIPR2 vasoactive intestinal peptide receptor 2