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TSHR

—Thyroid Stimulating Hormone Receptor

Chromosome: 14

Location: 14:80954989-81146306

OMIM: 603372

Ensembl: ENSG00000165409

Official·OMIM:603372 Official·ENSG00000165409

Encodes thyroid-stimulating hormone receptor. Mutations cause congenital hypothyroidism and hyperthyroidism.

Treatment Roadmap — TSHR

Preclinical

Phase 1

Phase 2

Phase 3

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