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ABHD12

Gene

abhydrolase domain containing 12, lysophospholipase

HGNCHGNC:15868EnsemblENSG00000100997NCBI Gene26090
Locus: gene with protein productLocation: 20p11.21

Also known as

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

Also known asC20orf22 · DKFZP434P106 · dJ965G21.2 · BEM46L2 · ABHD12A
View full nomenclature history (7)
Previous symbolsC20orf22
Alias symbolsDKFZP434P106, dJ965G21.2, BEM46L2, ABHD12A
Previous nameschromosome 20 open reading frame 22, abhydrolase domain containing 12

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
Optic Atrophy
Optic Atrophy, Hereditary, Leber
Retinitis Pigmentosa

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.

Abhydrolase domain containing2-arachidonoylglycerol hydrolases

Provenance

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