RESF1

Gene

retroelement silencing factor 1

HGNCHGNC:25559 EnsemblENSG00000174718 NCBI Gene55196

Locus: gene with protein productLocation: 12p11.21

Also known as

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

Also known asC12orf35 · FLJ20696 · FLJ10652 · UTA2-1 · GET

View full nomenclature history (8)

Previous symbolsC12orf35

Alias symbolsFLJ20696, FLJ10652, UTA2-1, GET

Previous namesKIAA1551, chromosome 12 open reading frame 35

Alias namesgonad expressed transcript

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.

Thyroid Diseases

Kidney Diseases

Neoplasms

Amyotrophic Lateral Sclerosis

Miyoshi myopathy

Head and Neck Neoplasms

Adjustment Disorders

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.

Minor histocompatibility antigens

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.