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FANCA

—FA Complementation Group A

Chromosome: 16

Location: 16:89726683-89816977

OMIM: 607139

Ensembl: ENSG00000187741

Official·OMIM:607139 Official·ENSG00000187741

Encodes Fanconi anemia DNA repair protein. Mutations cause Fanconi anemia type A.

Treatment Roadmap — FANCA

Preclinical

Phase 1

4 trial

Phase 2

18 trial

Phase 3

Approved

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

Associated Diseases

Fanconi Anemia

Autosomal RecessivePrevalence: 1/160000hematologic

Official·OMIM:227650 Official·ORPHA84

Summary

Clinical Trial

Approved Therapy

Registered Variant