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INS

—Insulin

Chromosome: 11

Location: 11:2159779-2161221

OMIM: 176730

Ensembl: ENSG00000254647

Official·OMIM:176730 Official·ENSG00000254647

Encodes insulin hormone. Mutations cause neonatal diabetes and MODY type 10.

Treatment Roadmap — INS

Preclinical

Phase 1

17 trial

Phase 2

35 trial

Phase 3

14 trial

Approved

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

Associated Diseases

Neonatal Diabetes

Autosomal DominantPrevalence: 1/100000endocrine

Official·OMIM:606176 Official·ORPHA224

Summary

343

Clinical Trial

Approved Therapy

Registered Variant