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CRX

Gene

cone-rod homeobox

HGNCHGNC:2383EnsemblENSG00000105392NCBI Gene1406
Locus: gene with protein productLocation: 19q13.33

Also known as

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

Also known asCORD2 · CRD · LCA7 · OTX3
View full nomenclature history (5)
Previous symbolsCORD2
Alias symbolsCRD, LCA7, OTX3
Alias namesorthodenticle homeobox 3

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.

Leber Congenital Amaurosis
Retinitis Pigmentosa
Cone rod dystrophy
Cone-rod dystrophy
Neurodegenerative 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.

PRD class homeoboxes and pseudogenes

Provenance

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