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EPS8L2

Gene

EPS8 signaling adaptor L2

HGNCHGNC:21296EnsemblENSG00000177106NCBI Gene64787
Locus: gene with protein productLocation: 11p15.5

Also known as

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

Also known asFLJ21935 · FLJ22171 · MGC3088
View full nomenclature history (6)
Alias symbolsFLJ21935, FLJ22171, MGC3088
Previous namesEPS8-like 2, EPS8 like 2
Alias namesEpidermal growth factor receptor kinase substrate 8-like protein 2

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.

Hearing loss, autosomal recessive
Deafness
Ovarian dysfunction
Non-syndromic genetic deafness
Genetic Diseases, Inborn
Nonsyndromic genetic hearing loss
Meniere's Disease

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.

EPS8 signaling adaptor family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-11-09.
Open TargetsGene–disease associations from the Open Targets Platform.