abnormal thyroid physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002876
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23 gene mutations causing the abnormal thyroid physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA5 ATP-binding cassette, sub-family A (ABC1), member 5
AIRE autoimmune regulator
ATCAY ataxia, cerebellar, Cayman type
CGA glycoprotein hormones, alpha polypeptide
DIO1 deiodinase, iodothyronine, type I
DUOX2 dual oxidase 2
FAS Fas cell surface death receptor
GFRA4 GDNF family receptor alpha 4
GHR growth hormone receptor
GLIS3 GLIS family zinc finger 3
HPN hepsin
LEP leptin
LHX3 LIM homeobox 3
LRPAP1 low density lipoprotein receptor-related protein associated protein 1
MED1 mediator complex subunit 1
NCOR1 nuclear receptor corepressor 1
RUNX2 runt-related transcription factor 2
THRA thyroid hormone receptor, alpha
THRB thyroid hormone receptor, beta
TK1 thymidine kinase 1, soluble
TPO thyroid peroxidase
TPST2 tyrosylprotein sulfotransferase 2
TSHR thyroid stimulating hormone receptor