Primary Hypothyroidism Gene Set
Genes
18 genes associated with the disease Primary Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
BRD2
|
bromodomain containing 2
|
|
CTLA4
|
cytotoxic T-lymphocyte-associated protein 4
|
|
CTNS
|
cystinosin, lysosomal cystine transporter
|
|
DDOST
|
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit (non-catalytic)
|
|
FSHR
|
follicle stimulating hormone receptor
|
|
GH1
|
growth hormone 1
|
|
GNAS
|
GNAS complex locus
|
|
NKX2-1
|
NK2 homeobox 1
|
|
PSMB9
|
proteasome (prosome, macropain) subunit, beta type, 9
|
|
SLC26A4
|
solute carrier family 26 (anion exchanger), member 4
|
|
SLC30A10
|
solute carrier family 30, member 10
|
|
SLCO1C1
|
solute carrier organic anion transporter family, member 1C1
|
|
STAT1
|
signal transducer and activator of transcription 1, 91kDa
|
|
TPO
|
thyroid peroxidase
|
|
TRHR
|
thyrotropin-releasing hormone receptor
|
|
TSHB
|
thyroid stimulating hormone, beta
|
|
TSHR
|
thyroid stimulating hormone receptor
|
|
VEGFA
|
vascular endothelial growth factor A
|
