thyroid hormone resistance syndrome Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [LS]. (Human Disease Ontology, DOID_11633)
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32 genes co-occuring with the disease thyroid hormone resistance syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
THRB thyroid hormone receptor, beta 3.11799
TXNRD2 thioredoxin reductase 2 2.2685
THRA thyroid hormone receptor, alpha 1.86827
TRH thyrotropin-releasing hormone 1.71271
ZNF764 zinc finger protein 764 1.59608
TSHB thyroid stimulating hormone, beta 1.40351
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter) 1.16949
THRSP thyroid hormone responsive 1.11856
OPN1MW2 opsin 1 (cone pigments), medium-wave-sensitive 2 1.11309
SHBG sex hormone-binding globulin 1.09671
OPN1LW opsin 1 (cone pigments), long-wave-sensitive 1.0732
OPN1MW opsin 1 (cone pigments), medium-wave-sensitive 1.0627
IGFALS insulin-like growth factor binding protein, acid labile subunit 0.846669
SERPINA7 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 7 0.820026
TRHR thyrotropin-releasing hormone receptor 0.787213
FAM195A family with sequence similarity 195, member A 0.752898
TG thyroglobulin 0.559062
F2R coagulation factor II (thrombin) receptor 0.514186
PROP1 PROP paired-like homeobox 1 0.501909
SHOX short stature homeobox 0.461261
TTR transthyretin 0.361502
CREB1 cAMP responsive element binding protein 1 0.292975
IGF1 insulin-like growth factor 1 (somatomedin C) 0.264785
CREBBP CREB binding protein 0.249257
FTL ferritin, light polypeptide 0.233183
FTH1 ferritin, heavy polypeptide 1 0.233183
PAX8 paired box 8 0.226952
POMC proopiomelanocortin 0.197099
GH1 growth hormone 1 0.18591
NCOR2 nuclear receptor corepressor 2 0.183541
GHR growth hormone receptor 0.178403
SST somatostatin 0.174093