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FLNB

—Filamin B

Chromosome: 3

Location: 3:58008398-58172251

OMIM: 603381

Ensembl: ENSG00000136068

Official·OMIM:603381 Official·ENSG00000136068

Encodes filamin B cytoskeletal protein. Mutations cause Larsen syndrome.

Treatment Roadmap — FLNB

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

Larsen Syndrome

Autosomal DominantPrevalence: 1/100000skeletal

Official·OMIM:150250 Official·ORPHA503

Summary

Clinical Trial

Approved Therapy

Registered Variant