increased triiodothyronine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater amount of a thyroid hormone 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_0005474)
External Link
Similar Terms
Downloads & Tools


11 gene mutations causing the increased 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
DIO3 deiodinase, iodothyronine, type III
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