abnormal 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 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_0005472)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005472
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Genes

28 gene mutations causing the abnormal 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
NR1I3 nuclear receptor subfamily 1, group I, member 3
PAX8 paired box 8
RUNX2 runt-related transcription factor 2
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SLCO1C1 solute carrier organic anion transporter family, member 1C1
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SSFA2 sperm specific antigen 2
TG thyroglobulin
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
TRHR thyrotropin-releasing hormone receptor
TSHR thyroid stimulating hormone receptor
TTR transthyretin
UCP1 uncoupling protein 1 (mitochondrial, proton carrier)
VIPR2 vasoactive intestinal peptide receptor 2