2 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
βGeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
39PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
RNA bindingribosomal small subunit biogenesisnucleolusnucleoplasmneurodegenerative diseasegliomanasopharyngeal carcinomanon-small cell lung carcinoma
Based on limited published evidence, RRP36 is a nucleolar protein essential for early pre-rRNA processing and ribosomal small subunit (40S) biogenesis. RRP36 functions within 90S preribosomal particles to facilitate early cleavages of 35S pre-rRNA, leading to mature 18S rRNA production 1. This function is evolutionarily conserved across eukaryotes. RRP36 recruitment depends on UTP-A and UTP-B subcomplexes but not on U3 snoRNP incorporation 1. Additionally, RRP36 has been identified as a hub gene in ribosome biogenesis pathways potentially linking metabolic disease to cancer mechanisms 2.
1
RRP36 is a nucleolar 90S preribosome component required for early pre-rRNA cleavages and 18S rRNA maturation; function conserved across eukaryotes
PMID: 200385302
RRP36 identified as hub gene in ribosome biogenesis module associated with type 2 diabetes and cancer pathways
PMID: 35601016β Limited data available β This gene has 2 indexed publications. Summary and analysis may be incomplete.
neurodegenerative diseaseOpen Targets
nasopharyngeal carcinomaOpen Targets
non-small cell lung carcinomaOpen Targets
Alzheimer diseaseOpen Targets
breast cancerOpen Targets
congenital short bowel syndromeOpen Targets
lung adenocarcinomaOpen Targets
type 2 diabetes mellitusOpen Targets
Insulin resistanceOpen Targets
Miyoshi myopathyOpen Targets
multiple sclerosisOpen Targets
neuroblastomaOpen Targets
Parkinson diseaseOpen Targets
spinocerebellar ataxia type 2Open Targets
type 1 diabetes mellitusOpen Targets
familial pancreatic carcinomaOpen Targets
Uveal MelanomaOpen Targets
No pathogenic variants reported on ClinVar for this gene.