Thyroid Hypoplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Developmental hypoplasia of the thyroid gland. (Human Phenotype Ontology, HP_0005990)
External Link https://www.disgenet.org/browser/0/1/0/C0151516
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Genes

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

Symbol Name
ADAMTSL1 ADAMTS-like 1
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
FOXE1 forkhead box E1
GLI3 GLI family zinc finger 3
KAT6B K(lysine) acetyltransferase 6B
NKX2-5 NK2 homeobox 5
PAX8 paired box 8
POLR1C polymerase (RNA) I polypeptide C, 30kDa
POLR1D polymerase (RNA) I polypeptide D, 16kDa
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TCOF1 Treacher Collins-Franceschetti syndrome 1
TPO thyroid peroxidase
TSHR thyroid stimulating hormone receptor