Thyroid Dysgenesis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1563716
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Genes

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

Symbol Name
CDCA8 cell division cycle associated 8
DNAJC17 DnaJ (Hsp40) homolog, subfamily C, member 17
DUOX1 dual oxidase 1
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
FOXE1 forkhead box E1
GLI3 GLI family zinc finger 3
GLIS3 GLIS family zinc finger 3
HLA-A major histocompatibility complex, class I, A
ISL1 ISL LIM homeobox 1
JAG1 jagged 1
NKX2-1 NK2 homeobox 1
NKX2-5 NK2 homeobox 5
NTN1 netrin 1
PAX8 paired box 8
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC5A5 solute carrier family 5 (sodium/iodide cotransporter), member 5
TAZ tafazzin
THRB thyroid hormone receptor, beta
TSHB thyroid stimulating hormone, beta
TSHR thyroid stimulating hormone receptor
TTF1 transcription termination factor, RNA polymerase I
TTF2 transcription termination factor, RNA polymerase II
TUBB1 tubulin, beta 1 class VI
WWTR1 WW domain containing transcription regulator 1