RP1

Gene

RP1 axonemal microtubule associated

HGNCHGNC:10263 EnsemblENSG00000104237 NCBI Gene6101

Locus: gene with protein productLocation: 8q11.23-q12.1

Also known as

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

Also known asDCDC4A · ORP1

View full nomenclature history (6)

Alias symbolsDCDC4A, ORP1

Previous namesretinitis pigmentosa 1 (autosomal dominant), RP1, axonemal microtubule associated

Alias namesdoublecortin domain containing 4A, oxygen-regulated protein 1

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

Genetic Diseases, Inborn

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.

Doublecortin superfamily

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.