LINGO4

Gene

leucine rich repeat and Ig domain containing 4

HGNCHGNC:31814 EnsemblENSG00000213171 NCBI Gene339398

Locus: gene with protein productLocation: 1q21.3

Also known as

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

Also known asLRRN6D

View full nomenclature history (2)

Previous symbolsLRRN6D

Previous namesleucine rich repeat neuronal 6D

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.

Speech Disorders

Asthma

Sleep Initiation and Maintenance Disorders

Colitis, Ulcerative

Inflammatory Bowel Diseases

Coronary Artery Disease

Lower respiratory tract disorder

Venous Thrombosis

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.

I-set domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.