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MYBBP1A

Gene

MYB binding protein 1a

HGNCHGNC:7546EnsemblENSG00000132382NCBI Gene10514
Locus: gene with protein productLocation: 17p13.2

Also known as

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

Also known asP160 · PAP2 · FLJ37886 · Pol5
View full nomenclature history (6)
Alias symbolsP160, PAP2, FLJ37886, Pol5
Previous namesMYB binding protein (P160) 1a
Alias namesp53-activated 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.

Neurodegenerative Diseases
Non-immune hydrops fetalis
Heart Septal Defects, Ventricular
Lysosomal Storage Diseases
Meniere's Disease
Autistic Disorder
Neoplasms
Carcinoma, Hepatocellular
Placental abruption

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.

Armadillo like helical domain containingB-WICH chromatin-remodelling complex subunits

Provenance

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