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HNF1A

—HNF1 Homeobox A

Chromosome: 12

Location: 12:120978543-121002512

OMIM: 142410

Ensembl: ENSG00000135100

Official·OMIM:142410 Official·ENSG00000135100

Encodes hepatocyte nuclear factor 1-alpha. Mutations cause MODY type 3.

Treatment Roadmap — HNF1A

Preclinical

Phase 1

1 trial

Phase 2

1 trial

Phase 3

Approved

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

Associated Diseases

MODY Type 3

Autosomal DominantPrevalence: 1/10000endocrine

Official·OMIM:600496 Official·ORPHA552

Summary

Clinical Trial

Approved Therapy

Registered Variant