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SERPINC1

—Serpin Family C Member 1

Chromosome: 1

Location: 1:173903414-173917543

OMIM: 107300

Ensembl: ENSG00000117601

Official·OMIM:107300 Official·ENSG00000117601

Encodes antithrombin III. Mutations cause hereditary antithrombin deficiency.

Treatment Roadmap — SERPINC1

Preclinical

Phase 1

Phase 2

1 trial

Phase 3

2 trial

Approved

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

Associated Diseases

Hereditary Antithrombin Deficiency

Autosomal DominantPrevalence: 1/5000hematologic

Official·OMIM:613118 Official·ORPHA82

Summary

Clinical Trial

Approved Therapy

Registered Variant