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MAPRE2

Gene

microtubule associated protein RP/EB family member 2

HGNCHGNC:6891EnsemblENSG00000166974NCBI Gene10982
Locus: gene with protein productLocation: 18q12.1-q12.2

Also known as

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

Also known asRP1 · EB1 · EB2
View full nomenclature history (4)
Alias symbolsRP1, EB1, EB2
Alias namesAPC-binding protein EB1

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
Brugada syndrome
Developmental Disabilities
Ovarian dysfunction
Intestinal Diseases
Liver Diseases

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.

Microtubule associated protein RP/EB family

Provenance

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