RETREG3

Gene

reticulophagy regulator family member 3

HGNCHGNC:27258 EnsemblENSG00000141699 NCBI Gene162427

Locus: gene with protein productLocation: 17q21.2

Also known as

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

Also known asFAM134C · DKFZp686B1036 · FLJ33806

View full nomenclature history (5)

Previous symbolsFAM134C

Alias symbolsDKFZp686B1036, FLJ33806

Previous namesfamily with sequence similarity 134, member C, family with sequence similarity 134 member C

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 central nervous system malformation

Genetic Diseases, Inborn

Diabetes Mellitus, Type 2

Diabetes Mellitus

Autistic Disorder

Helicobacter Infections

Retinitis Pigmentosa

Leber Congenital Amaurosis

Coronary Artery Disease

Cone rod dystrophy

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 2024-08-09.

Open TargetsGene–disease associations from the Open Targets Platform.