RP2

Gene

RP2 activator of ARL3 GTPase

HGNCHGNC:10274 EnsemblENSG00000102218 NCBI Gene6102

Locus: gene with protein productLocation: Xp11.3

Also known as

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

Also known asTBCCD2 · NME10 · NM23-H10

View full nomenclature history (5)

Alias symbolsTBCCD2, NME10, NM23-H10

Previous namesretinitis pigmentosa 2 (X-linked recessive), RP2, ARL3 GTPase activating protein

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.

Retinitis Pigmentosa

Leber Congenital Amaurosis

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.