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PKD1

—Polycystin 1 Transient Receptor Potential Channel Interacting

Chromosome: 16

Location: 16:2088708-2135898

OMIM: 601313

Ensembl: ENSG00000008710

Official·OMIM:601313 Official·ENSG00000008710

Encodes polycystin-1 protein. Mutations cause autosomal dominant polycystic kidney disease.

Treatment Roadmap — PKD1

Preclinical

Phase 1

Phase 2

1 trial

Phase 3

Approved

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

Associated Diseases

Autosomal Dominant Polycystic Kidney Disease

Autosomal DominantPrevalence: 1/1000renal

Official·OMIM:173900 Official·ORPHA730

Summary

Clinical Trial

Approved Therapy

Registered Variant