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FERD3L

Gene

Fer3 like bHLH transcription factor

HGNCHGNC:16660EnsemblENSG00000146618NCBI Gene222894
Locus: gene with protein productLocation: 7p21.1

Also known as

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

Also known asNATO3 · N-TWIST · bHLHa31
View full nomenclature history (5)
Alias symbolsNATO3, N-TWIST, bHLHa31
Previous namesFer3-like (Drosophila), Fer3-like bHLH 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.

Macular Degeneration
Aortic Valve Stenosis
Wounds and Injuries
Brain Diseases
Carcinoma, Squamous Cell
Subarachnoid Hemorrhage

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.

Basic helix-loop-helix proteins

Provenance

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