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PCMTD2

Gene

protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2

HGNCHGNC:15882EnsemblENSG00000203880NCBI Gene55251
Locus: gene with protein productLocation: 20q13.33

Also known as

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

Also known asC20orf36 · FLJ10883
View full nomenclature history (3)
Previous symbolsC20orf36
Alias symbolsFLJ10883
Previous nameschromosome 20 open reading frame 36

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.

Coffee consumption
Neuroendocrine Tumors
Colorectal Neoplasms
Schizophrenia
Ovarian carcinoma
Bacteremia
Attention Deficit Disorder with Hyperactivity
Neoplasms
Alzheimer'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.

7BS protein methyltransferasesIsoaspartate methyltransferases

Provenance

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