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CYP1B1

—Cytochrome P450 Family 1 Subfamily B Member 1

Chromosome: 2

Location: 2:38066973-38109902

OMIM: 601771

Ensembl: ENSG00000138061

Official·OMIM:601771 Official·ENSG00000138061

Encodes cytochrome P450 enzyme. Mutations cause primary congenital glaucoma.

Treatment Roadmap — CYP1B1

Preclinical

Phase 1

1 trial

Phase 2

Phase 3

Approved

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

Associated Diseases

Primary Congenital Glaucoma

Autosomal RecessivePrevalence: 1/10000ophthalmologic

Official·OMIM:231300 Official·ORPHA98976

Summary

Clinical Trial

Approved Therapy

Registered Variant