Subclinical Hypothyroidism Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0271790
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Genes

34 genes associated with the disease Subclinical Hypothyroidism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
ANGPTL3 angiopoietin-like 3
ANPEP alanyl (membrane) aminopeptidase
APOA1 apolipoprotein A-I
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1
BEST1 bestrophin 1
BMP4 bone morphogenetic protein 4
CRP C-reactive protein, pentraxin-related
DMD dystrophin
DUOX2 dual oxidase 2
FGF23 fibroblast growth factor 23
GDF15 growth differentiation factor 15
GNAS GNAS complex locus
IFNA1 interferon, alpha 1
IFNA13 interferon, alpha 13
LIF leukemia inhibitory factor
LPA lipoprotein, Lp(a)
LRPAP1 low density lipoprotein receptor-related protein associated protein 1
NUCB2 nucleobindin 2
PAX8 paired box 8
PDE8B phosphodiesterase 8B
PRL prolactin
RARRES2 retinoic acid receptor responder (tazarotene induced) 2
RBP4 retinol binding protein 4, plasma
RYR2 ryanodine receptor 2 (cardiac)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
TG thyroglobulin
TNF tumor necrosis factor
TPO thyroid peroxidase
TRH thyrotropin-releasing hormone
TSHR thyroid stimulating hormone receptor
XBP1 X-box binding protein 1