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RNPC3

Gene

RNA binding region (RNP1, RRM) containing 3

HGNCHGNC:18666EnsemblENSG00000185946NCBI Gene55599
Locus: gene with protein productLocation: 1p21.1

Also known as

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

Also known asKIAA1839 · FLJ20008 · RBM40 · SNRNP65
View full nomenclature history (5)
Alias symbolsKIAA1839, FLJ20008, RBM40, SNRNP65
Alias namesU11/U12 snRNP 65K

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.

Neurodegenerative Diseases
Dentures
Gastritis, Atrophic
Genetic Diseases, Inborn
Lupus Erythematosus, Systemic

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.

RNA binding motif containingU11/U12 di-snRNP

Provenance

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