thyrotoxicosis Gene Set

Dataset DISEASES Experimental Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A thyroid gland disease that is characterized by excess thyroid hormone. (Human Disease Ontology, DOID_7997)
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Genes

19 genes associated with the disease thyrotoxicosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
MICA MHC class I polypeptide-related sequence A 2.37659
HLA-DPB1 major histocompatibility complex, class II, DP beta 1 2.37659
C6ORF15 chromosome 6 open reading frame 15 2.19204
GPR174 G protein-coupled receptor 174 1.84115
TSHR thyroid stimulating hormone receptor 1.52751
HLA-A major histocompatibility complex, class I, A 1.37597
C1QTNF6 C1q and tumor necrosis factor related protein 6 1.35143
SLAMF6 SLAM family member 6 1.27521
CTLA4 cytotoxic T-lymphocyte-associated protein 4 1.22898
HLA-J major histocompatibility complex, class I, J (pseudogene) 1.07383
MUC21 mucin 21, cell surface associated 0.965481
CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal) 0.965481
ABCF1 ATP-binding cassette, sub-family F (GCN20), member 1 0.965481
FCRL3 Fc receptor-like 3 0.945428
ITPR3 inositol 1,4,5-trisphosphate receptor, type 3 0.850113
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) 0.69843
RNASET2 ribonuclease T2 0.647573
TG thyroglobulin 0.537125
BACH2 BTB and CNC homology 1, basic leucine zipper transcription factor 2 0.197766