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TG

—Thyroglobulin

Chromosome: 8

Location: 8:132866958-133134903

OMIM: 188450

Ensembl: ENSG00000042832

Official·OMIM:188450 Official·ENSG00000042832

Encodes thyroglobulin protein. Mutations cause congenital goitrous hypothyroidism.

Treatment Roadmap — TG

Preclinical

Phase 1

8 trial

Phase 2

8 trial

Phase 3

6 trial

Approved

Clinical trials have approximately 10% success rate. This roadmap shows the current status, not guaranteed outcomes.

Associated Diseases

Congenital Hypothyroidism

Autosomal RecessivePrevalence: 1/3000endocrine

Official·OMIM:275200 Official·ORPHA442

Summary

Clinical Trial

Approved Therapy

Registered Variant