Iodine Deficiency Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0342199
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Genes

22 genes associated with the disease Iodine Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
BRAF B-Raf proto-oncogene, serine/threonine kinase
DIO1 deiodinase, iodothyronine, type I
DIO2 deiodinase, iodothyronine, type II
DLL1 delta-like 1 (Drosophila)
FABP7 fatty acid binding protein 7, brain
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
KDR kinase insert domain receptor
MAP1B microtubule-associated protein 1B
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NKX2-1 NK2 homeobox 1
NOTCH1 notch 1
NRCAM neuronal cell adhesion molecule
RBPJ recombination signal binding protein for immunoglobulin kappa J region
RET ret proto-oncogene
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC5A5 solute carrier family 5 (sodium/iodide cotransporter), member 5
TFF3 trefoil factor 3 (intestinal)
TG thyroglobulin
TNF tumor necrosis factor
TSHR thyroid stimulating hormone receptor
VEGFA vascular endothelial growth factor A