abnormal thyroid-stimulating hormone level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous concentration of the hormone that stimulates the growth and function of the thyroid gland (Mammalian Phenotype Ontology, MP_0003971)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003971
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25 gene mutations causing the abnormal thyroid-stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CGA glycoprotein hormones, alpha polypeptide
DIO2 deiodinase, iodothyronine, type II
DIO3 deiodinase, iodothyronine, type III
DUOX2 dual oxidase 2
FOXE1 forkhead box E1
HOXA5 homeobox A5
INSM1 insulinoma-associated 1
LHX3 LIM homeobox 3
LHX4 LIM homeobox 4
MED1 mediator complex subunit 1
NCOA1 nuclear receptor coactivator 1
NKX2-1 NK2 homeobox 1
PAX8 paired box 8
PROP1 PROP paired-like homeobox 1
RUNX2 runt-related transcription factor 2
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
SOX2 SRY (sex determining region Y)-box 2
SOX3 SRY (sex determining region Y)-box 3
TG thyroglobulin
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
TPO thyroid peroxidase
TRH thyrotropin-releasing hormone
TSHR thyroid stimulating hormone receptor
VGF VGF nerve growth factor inducible