PRKN
HGNC:8607 · SaudiVarKB evidence summary derived from retained literature mentions.
6Gene mentions
6Publications
0Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in PRKN publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| Parkinson disease | — | 3 | 3 |
| Alzheimer disease | — | 1 | 1 |
| neurodevelopmental disorder | HP:0012759 | 1 | 1 |
Linked variants
Variants normalized to PRKN| 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 |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
| Not specified | — | 1,322 | 1 |
Supporting publications
6 records- 2025CNV-Finder: Streamlining Copy Number Variation Discovery.bioRxiv : the preprint server for biologyPubMed ↗
- 2025Investigating the link between microplastic exposure (benzyl butyl phthalate) and neurodegenerative diseases using high-performance computational toxicology.Toxicology researchPubMed ↗
- 2024Oxidative Stress and Dopaminergic Metabolism: A Major PD Pathogenic Mechanism and Basis of Potential Antioxidant Therapies.CNS & neurological disorders drug targetsPubMed ↗
- 2023Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.Movement disorders : official journal of the Movement Disorder SocietyPubMed ↗
- 2018Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases.Molecular genetics and metabolismPubMed ↗
- 2014C19orf12 mutation leads to a pallido-pyramidal syndrome.GenePubMed ↗