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TSC1

—TSC Complex Subunit 1

Chromosome: 9

Location: 9:132891348-132946874

OMIM: 605284

Ensembl: ENSG00000165699

Official·OMIM:605284 Official·ENSG00000165699

Encodes hamartin protein. Mutations cause tuberous sclerosis.

Treatment Roadmap — TSC1

Preclinical

Phase 1

2 trial

Phase 2

7 trial

Phase 3

Approved

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

Associated Diseases

Tuberous Sclerosis Complex

Autosomal DominantPrevalence: 1/6000oncologic

Official·OMIM:191100 Official·ORPHA805

Summary

Clinical Trial

Approved Therapy

Registered Variant