hypothyroidism Gene Set

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

21 genes associated with the disease hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ASIC2 acid sensing (proton gated) ion channel 2
C1QTNF6 C1q and tumor necrosis factor related protein 6
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DIO1 deiodinase, iodothyronine, type I
DIO2 deiodinase, iodothyronine, type II
DIO3 deiodinase, iodothyronine, type III
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HSPA1B heat shock 70kDa protein 1B
HSPA1L heat shock 70kDa protein 1-like
INSR insulin receptor
LTA lymphotoxin alpha
MTF1 metal-regulatory transcription factor 1
PDE8B phosphodiesterase 8B
SH2B3 SH2B adaptor protein 3
TNF tumor necrosis factor
TPO thyroid peroxidase
TSHB thyroid stimulating hormone, beta
TSHR thyroid stimulating hormone receptor
VAV3 vav 3 guanine nucleotide exchange factor
ZNF804B zinc finger protein 804B