decreased circulating triiodothyronine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced 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_0005479)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005479
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Genes

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

Symbol Name
ARRDC3 arrestin domain containing 3
CRYM crystallin, mu
DIO3 deiodinase, iodothyronine, type III
EDN2 endothelin 2
FRK fyn-related Src family tyrosine kinase
GHR growth hormone receptor
MED1 mediator complex subunit 1
NCOR1 nuclear receptor corepressor 1
PAX8 paired box 8
SSFA2 sperm specific antigen 2
TG thyroglobulin
THRA thyroid hormone receptor, alpha
TSHR thyroid stimulating hormone receptor
TTR transthyretin