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HAX1

—HCLS1 Associated Protein X-1

Chromosome: 1

Location: 1:154272326-154275882

OMIM: 605998

Ensembl: ENSG00000143575

Official·OMIM:605998 Official·ENSG00000143575

Encodes anti-apoptotic protein. Mutations cause Kostmann syndrome (severe congenital neutropenia).

Treatment Roadmap — HAX1

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

Severe Congenital Neutropenia

Autosomal RecessivePrevalence: 1/200000hematologic

Official·OMIM:202700 Official·ORPHA486

Summary

Clinical Trial

Approved Therapy

Registered Variant