NRAP
HGNC:7988 · SaudiVarKB evidence summary derived from retained literature mentions.
3Gene mentions
3Publications
0Linked variants
2Associated phenotypes
Associated phenotypes
Co-mentioned in NRAP publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| cardiomyopathy | HP:0001638 | 2 | 2 |
| intellectual disability | HP:0001249 | 1 | 1 |
Linked variants
Variants normalized to NRAP| 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 | — | — | 1 |
| Not specified | — | 12 | 1 |
| Saudi Arabia | — | 1,000 | 1 |
Supporting publications
3 records- 2026Reduced Penetrance and Variable Expression of Dilated Cardiomyopathy Associated With Homozygous Truncating Variants in NRAP Gene.Clinical geneticsPubMed ↗
- 2023Genetic Insights from Consanguineous Cardiomyopathy Families.GenesPubMed ↗
- 2017The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes.Human geneticsPubMed ↗