Thyroid Agenesis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The congenital absence of the thyroid gland. (Human Phenotype Ontology, HP_0008191)
External Link https://www.disgenet.org/browser/0/1/0/C0749420
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Genes

11 genes associated with the disease Thyroid Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
FOXE1 forkhead box E1
IGSF1 immunoglobulin superfamily, member 1
KAT6B K(lysine) acetyltransferase 6B
NKX2-1 NK2 homeobox 1
NKX2-5 NK2 homeobox 5
PAX8 paired box 8
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TG thyroglobulin
TSHR thyroid stimulating hormone receptor
TTF2 transcription termination factor, RNA polymerase II