CD151
HGNC:1630 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
2Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in CD151 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| nephrotic syndrome | — | 2 | 2 |
| hearing loss | HP:0000365 | 1 | 1 |
Linked variants
Variants normalized to CD151Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
| Saudi Arabia · Riyadh | — | 206 | 1 |
Supporting publications
2 records- 2024Nephrotic syndrome: Pretibial epidermolysis bullosa in a patient with CD151 tetraspanin defect: A case report.International journal of health sciencesPubMed ↗
- 2021The Frequency of Genetic Mutations in Pediatric Patients Diagnosed with Nephrotic Syndrome: A Single-Center Retrospective Study in Saudi Arabia.Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi ArabiaPubMed ↗