Goiter Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A thyroid gland disease that involves an abnormal enlargement of the thyroid gland. (Human Disease Ontology, DOID_12176)
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16 genes associated with the Goiter phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
BRAF B-Raf proto-oncogene, serine/threonine kinase
C4A complement component 4A (Rodgers blood group)
CAPZB capping protein (actin filament) muscle Z-line, beta
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
FGF7 fibroblast growth factor 7
FOXI1 forkhead box I1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL13 interleukin 13
IL5 interleukin 5
IL6 interleukin 6
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
LRPAP1 low density lipoprotein receptor-related protein associated protein 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TSHR thyroid stimulating hormone receptor