hypothyroidism Gene Set

Dataset DISEASES Experimental Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A deficiency of thyroid hormone. (Experimental Factor Ontology, EFO_0004705)
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Genes

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

Symbol Name Standardized Value
FOXE1 forkhead box E1 1.32252
RSBN1 round spermatid basic protein 1 0.932337
SH2B3 SH2B adaptor protein 3 0.85991
VAV3 vav 3 guanine nucleotide exchange factor 0.641775
C6ORF15 chromosome 6 open reading frame 15 0.52461
PDE8B phosphodiesterase 8B 0.197766
ZBTB10 zinc finger and BTB domain containing 10 0.126165
INSR insulin receptor 0.100789
SACS sacsin molecular chaperone 0.100789
ASIC2 acid sensing (proton gated) ion channel 2 0.064973
ZNF804B zinc finger protein 804B 0.064973
CTLA4 cytotoxic T-lymphocyte-associated protein 4 0.064973
C1QTNF6 C1q and tumor necrosis factor related protein 6 0.043246
MTF1 metal-regulatory transcription factor 1 0.043246