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SEMA6D

Gene

semaphorin 6D

HGNCHGNC:16770EnsemblENSG00000137872NCBI Gene80031
Locus: gene with protein productLocation: 15q21.1

Also known as

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

Also known asKIAA1479 · FLJ11598
View full nomenclature history (3)
Alias symbolsKIAA1479, FLJ11598
Previous namessema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 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.

Neurodegenerative Diseases
Restless Legs Syndrome
Attention Deficit Disorder with Hyperactivity
Substance-Related Disorders
Smoking initiation
Risk-taking behaviour
Smoking cessation
Marijuana Abuse
Sleep Initiation and Maintenance 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.

Semaphorins

Provenance

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