abnormal circulating triiodothyronine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the 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_0005476)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005476
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Genes

23 gene mutations causing the abnormal circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGRP agouti related neuropeptide
ARRDC3 arrestin domain containing 3
CPE carboxypeptidase E
CRYM crystallin, mu
DIO1 deiodinase, iodothyronine, type I
DIO3 deiodinase, iodothyronine, type III
EDN2 endothelin 2
FRK fyn-related Src family tyrosine kinase
GHR growth hormone receptor
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial)
MED1 mediator complex subunit 1
NCOA1 nuclear receptor coactivator 1
NCOR1 nuclear receptor corepressor 1
PAX8 paired box 8
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SSFA2 sperm specific antigen 2
TG thyroglobulin
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
TSHR thyroid stimulating hormone receptor
TTR transthyretin
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
VIPR2 vasoactive intestinal peptide receptor 2