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HNF4A

—Hepatocyte Nuclear Factor 4 Alpha

Chromosome: 20

Location: 20:44355439-44432845

OMIM: 600281

Ensembl: ENSG00000101076

Official·OMIM:600281 Official·ENSG00000101076

Encodes hepatocyte nuclear factor 4-alpha. Mutations cause MODY type 1.

Treatment Roadmap — HNF4A

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

MODY Type 1

Autosomal DominantPrevalence: 1/50000endocrine

Official·OMIM:125850 Official·ORPHA552

Summary

Clinical Trial

Approved Therapy

Registered Variant