Back to discover

NFIX

Gene

nuclear factor I X

HGNCHGNC:7788EnsemblENSG00000008441NCBI Gene4784
Locus: gene with protein productLocation: 19p13.13

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asNF1A
View full nomenclature history (3)
Alias symbolsNF1A
Previous namesnuclear factor I/X (CCAAT-binding transcription factor)
Alias namesCCAAT-binding transcription factor

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Genetic Diseases, Inborn
Craniosynostoses
Neurodevelopmental Disorders

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Nuclear factor I family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.