abnormal circulating triiodothyronine level Gene Set
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
|