RPL5
HGNC:10360 · SaudiVarKB evidence summary derived from retained literature mentions.
5Gene mentions
5Publications
2Linked variants
5Associated phenotypes
Associated phenotypes
Co-mentioned in RPL5 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| sickle cell disease | HP:0001878 | 1 | 1 |
| multiple sclerosis | — | 1 | 1 |
| familial hypercholesterolemia | HP:0003124 | 1 | 1 |
| stroke | — | 1 | 1 |
| cleft lip and palate | — | 1 | 1 |
Linked variants
Variants normalized to RPL5| Variant | HGVS / rsID | Articles | Mentions |
|---|---|---|---|
| p.Gly140Ser | p.Gly140Ser | 1 | 1 |
| rs6604026 | rs6604026 | 1 | 1 |
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | 100 | 1 |
| Not specified | — | 45 | 1 |
| Saudi Arabia | — | 22 | 1 |
| Saudi Arabia | — | 50 | 1 |
Supporting publications
5 records- 2025Integrated Bioinformatics Analysis of Differentially Expressed RNA-Binding Proteins in Human Gliomas.Cellular and molecular neurobiologyPubMed ↗
- 2021Identification of RPL5 gene variants and the risk of hepatic vein thrombosis in Saudi patients.Saudi medical journalPubMed ↗
- 2021Genetic Variants of RPL5 and RPL9 Genes among Saudi Patients Diagnosed with Thrombosis.Medical archives (Sarajevo, Bosnia and Herzegovina)PubMed ↗
- 2018Molecular analysis and genotype-phenotype correlation of Diamond-Blackfan anemia.Clinical geneticsPubMed ↗
- 2018Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease.Genetic testing and molecular biomarkersPubMed ↗