Hypothyroidism Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description A deficiency of thyroid hormone. (Experimental Factor Ontology, EFO_0004705)
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Genes

20 genes involed in the disease Hypothyroidism from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
SLC26A4 solute carrier family 26 (anion exchanger), member 4 5.0
TRHR thyrotropin-releasing hormone receptor 4.0
IRS4 insulin receptor substrate 4 4.0
PAX8 paired box 8 4.0
IYD iodotyrosine deiodinase 4.0
KMT2D lysine (K)-specific methyltransferase 2D 4.0
TSHB thyroid stimulating hormone, beta 4.0
NKX2-1 NK2 homeobox 1 4.0
NKX2-5 NK2 homeobox 5 4.0
GLIS3 GLIS family zinc finger 3 4.0
TSHR thyroid stimulating hormone receptor 4.0
THRA thyroid hormone receptor, alpha 4.0
TG thyroglobulin 4.0
IGSF1 immunoglobulin superfamily, member 1 4.0
FOXE1 forkhead box E1 4.0
DUOX2 dual oxidase 2 4.0
SLC5A5 solute carrier family 5 (sodium/iodide cotransporter), member 5 4.0
DUOXA2 dual oxidase maturation factor 2 4.0
TPO thyroid peroxidase 4.0
TBL1X transducin (beta)-like 1X-linked 4.0