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SEMA6A

Gene

semaphorin 6A

HGNCHGNC:10738EnsemblENSG00000092421NCBI Gene57556
Locus: gene with protein productLocation: 5q23.1

Also known as

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

Also known asSEMAQ · KIAA1368 · SEMA6A1 · SEMA · HT018
View full nomenclature history (7)
Previous symbolsSEMAQ
Alias symbolsKIAA1368, SEMA6A1, SEMA, HT018
Previous namessema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A
Alias namessema VIa

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
Bipolar Disorder
Essential Tremor
Lupus Erythematosus, Systemic
Sjogren's Syndrome
Hair color
Neuroendocrine Tumors

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.