SEMA5B

Gene

semaphorin 5B

HGNCHGNC:10737 EnsemblENSG00000082684 NCBI Gene54437

Locus: gene with protein productLocation: 3q21.1

Also known as

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

Also known asSEMAG · SemG · KIAA1445 · FLJ10372

View full nomenclature history (5)

Previous symbolsSEMAG

Alias symbolsSemG, KIAA1445, FLJ10372

Previous namessema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B

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.

Coronary Artery Disease

Atrial Fibrillation

Amino Acid Metabolism, Inborn Errors

Celiac Disease

Alcohol drinking

Seasonal allergic rhinitis

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 2023-03-15.

Open TargetsGene–disease associations from the Open Targets Platform.