ESAM

Gene

endothelial cell adhesion molecule

HGNCHGNC:17474 EnsemblENSG00000149564 NCBI Gene90952

Locus: gene with protein productLocation: 11q24.2

Also known as

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

Also known asW117m

View full nomenclature history (1)

Alias symbolsW117m

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.

Schizophrenia

Autism Spectrum Disorder

Anorexia Nervosa

Irritable Bowel Syndrome

Attention Deficit Disorder with Hyperactivity

Bipolar Disorder

Intelligence

Obsessive-Compulsive Disorder

Tourette's Syndrome

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.

V-set domain containingIgCAM CXADR-related subfamily

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.