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RAI1

Gene

retinoic acid induced 1

HGNCHGNC:9834EnsemblENSG00000108557NCBI Gene10743
Locus: gene with protein productLocation: 17p11.2

Also known as

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

Also known asSMCR · DKFZP434A139 · SMS · KIAA1820 · MGC12824
View full nomenclature history (6)
Previous symbolsSMCR
Alias symbolsDKFZP434A139, SMS, KIAA1820, MGC12824
Previous namesSmith-Magenis syndrome chromosome region

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.

Genetic Diseases, Inborn
Coffee consumption
Developmental Disabilities
Diabetes Mellitus, Type 2
Skin Neoplasms

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.

PHD finger proteins

Provenance

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