RPL9
HGNC:10369 · SaudiVarKB evidence summary derived from retained literature mentions.
4Gene mentions
4Publications
0Linked variants
6Associated phenotypes
Associated phenotypes
Co-mentioned in RPL9 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| intellectual disability | HP:0001249 | 1 | 1 |
| leukemia | — | 1 | 1 |
| diabetes mellitus | — | 1 | 1 |
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
| multiple sclerosis | — | 1 | 1 |
| COVID-19 | — | 1 | 1 |
Linked variants
Variants normalized to RPL9| Variant | HGVS / rsID | Articles | Mentions |
|---|
No normalized variants are linked to this gene.
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Not specified | — | 10 | 1 |
| Not specified | — | 19 | 1 |
| Saudi Arabia | — | 100 | 1 |
Supporting publications
4 records- 2025Identification of cell specific biomarkers for intellectual disability via single cell RNA sequencing and transcriptomic bioinformatics approaches.Scientific reportsPubMed ↗
- 2024Role of ribosomal pathways and comorbidity in COVID-19: Insight from SARS-CoV-2 proteins and host proteins interaction network analysis.HeliyonPubMed ↗
- 2023Potential Candidate Genes for Therapeutic Targeting in Chronic Myeloid Leukemia: A Pilot Study.Asian Pacific journal of cancer prevention : APJCPPubMed ↗
- 2021Genetic Variants of RPL5 and RPL9 Genes among Saudi Patients Diagnosed with Thrombosis.Medical archives (Sarajevo, Bosnia and Herzegovina)PubMed ↗