TG Chromosome 8

Thyroglobulin
307 variants 307 Health Risk

Upload your DNA to see your personal genotypes for variants in TG.

What This Gene Does
Thyroglobulin (Tg) is a glycoprotein homodimer produced predominantly by the thryroid gland. It acts as a substrate for the synthesis of thyroxine and triiodothyronine as well as the storage of the inactive forms of thyroid hormone and iodine. Thyroglobulin is secreted from the endoplasmic reticulum to its site of iodination, and subsequent thyroxine biosynthesis, in the follicular lumen. Mutations in this gene cause thyroid dyshormonogenesis, manifested as goiter, and are associated with moderate to severe congenital hypothyroidism. Polymorphisms in this gene are associated with susceptibility to autoimmune thyroid diseases (AITD) such as Graves disease and Hashimoto thryoiditis. [provided by RefSeq, Nov 2009]
Associated Conditions (16)
Iodotyrosyl coupling defect
Inborn genetic diseases
TG-related disorder
Autoimmune thyroid disease
susceptibility to
3
Thyroid cancer
nonmedullary
1
Ovarian serous cystadenocarcinoma
Congenital hypothyroidism
Acute myeloid leukemia
Lung cancer
Premature ovarian failure
Gastric cancer
Hypothyroidism
Key Variants
RS1022148195
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS111363334
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Inborn genetic diseases, Iodotyrosyl coupling defect
Health Risk
RS112300885
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114211101
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114305064
Conflicting classifications of pathogenicity
Inborn genetic diseases, TG-related disorder, Inborn genetic diseases
Health Risk
RS114322847
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114436500
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, TG-related disorder, Iodotyrosyl coupling defect
Health Risk
RS114477962
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114613744
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114781869
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
Health Risk
RS114875802
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
Health Risk
RS114944116
Conflicting classifications of pathogenicity
Iodotyrosyl coupling defect, Thyroid cancer, nonmedullary
Health Risk
All Variants (307)
RSID Category Clinical Significance Conditions
RS2491034194 Health Risk Likely pathogenic
RS2491035032 Health Risk Likely pathogenic TG-related disorder, TG-related disorder
RS2537735975 Health Risk Likely pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS376200169 Health Risk Likely pathogenic Congenital hypothyroidism, Iodotyrosyl coupling defect, Autoimmune thyroid disease
RS377652873 Health Risk Likely pathogenic
RS748654543 Health Risk Likely pathogenic
RS757080996 Health Risk Likely pathogenic
RS766130576 Health Risk Likely pathogenic Congenital hypothyroidism, Congenital hypothyroidism
RS767564345 Health Risk Likely pathogenic
RS769281672 Health Risk Likely pathogenic
RS775401701 Health Risk Likely pathogenic
RS898275076 Health Risk Likely pathogenic Iodotyrosyl coupling defect, TG-related disorder, Iodotyrosyl coupling defect
RS945798509 Health Risk Likely pathogenic
RS976187958 Health Risk Likely pathogenic
RS998036326 Health Risk Likely pathogenic Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
RS114157534 Health Risk Pathogenic
RS116726914 Health Risk Pathogenic TG-related disorder, TG-related disorder
RS1171241375 Health Risk Pathogenic
RS1181511105 Health Risk Pathogenic
RS1194583771 Health Risk Pathogenic
RS1195103622 Health Risk Pathogenic
RS121912646 Health Risk Pathogenic Iodotyrosyl coupling defect, Congenital hypothyroidism, Autoimmune thyroid disease
RS121912647 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS121912648 Health Risk Pathogenic Iodotyrosyl coupling defect, Congenital hypothyroidism, Autoimmune thyroid disease
RS1249844474 Health Risk Pathogenic
RS1255388549 Health Risk Pathogenic
RS1310897860 Health Risk Pathogenic
RS1373380416 Health Risk Pathogenic
RS137854433 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS1398373161 Health Risk Pathogenic Iodotyrosyl coupling defect, Autoimmune thyroid disease, susceptibility to
RS1410846026 Health Risk Pathogenic
RS1412480668 Health Risk Pathogenic Autoimmune thyroid disease, susceptibility to, 3
RS141306917 Health Risk Pathogenic Autoimmune thyroid disease, susceptibility to, 3
RS1426751404 Health Risk Pathogenic
RS1427839472 Health Risk Pathogenic
RS143023529 Health Risk Pathogenic
RS1440911824 Health Risk Pathogenic
RS144875913 Health Risk Pathogenic TG-related disorder, TG-related disorder
RS1448908452 Health Risk Pathogenic
RS1450178339 Health Risk Pathogenic
RS1464861162 Health Risk Pathogenic TG-related disorder, TG-related disorder
RS1554649344 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS1554657542 Health Risk Pathogenic
RS1587166863 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS1587178555 Health Risk Pathogenic Iodotyrosyl coupling defect, Congenital hypothyroidism, Iodotyrosyl coupling defect
RS1587678058 Health Risk Pathogenic Iodotyrosyl coupling defect, Iodotyrosyl coupling defect
RS1814692109 Health Risk Pathogenic Congenital hypothyroidism, Congenital hypothyroidism
RS1815438013 Health Risk Pathogenic
RS1815496874 Health Risk Pathogenic
RS1815564741 Health Risk Pathogenic
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