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RMND1

Gene

required for meiotic nuclear division 1 homolog

HGNCHGNC:21176EnsemblENSG00000155906NCBI Gene55005
Locus: gene with protein productLocation: 6q25.1

Also known as

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

Also known asC6orf96 · bA351K16.3 · FLJ20627 · RMD1
View full nomenclature history (6)
Previous symbolsC6orf96
Alias symbolsbA351K16.3, FLJ20627, RMD1
Previous namesrequired for meiotic nuclear division 1 homolog (S. cerevisiae), chromosome 6 open reading frame 96

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
Neurodegenerative Diseases
Mitochondrial Diseases
Kidney Failure, Chronic
Nephritis, Interstitial

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 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.