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ATP13A2 and Parkinson disease are reported together in 3 articles.
Gene
ATP13A2
- HGNC
- HGNC:30213
6articles
6mentions
0variants with confirmed gene link
Most co-reported phenotypes (articles)
Phenotype
Parkinson disease
280articles
280mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
3 records shown · first 60Computational association in parkinson's disease SNPs with brain structural and functional alterations.
PMID 40782224 | DOI 10.1007/s10048-025-00843-6 · Neurogenetics · 2025 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ATP13A2 | “SNCA, LRRK2, NURR1, ATP13A2, GSK3B, Parkin, PINK1, DJ-1, and UCHL1are the major genes involved and play a crucial role in the regulatory mechanisms and progression of PD.” | 0.98 | hgnc_dict_v1 |
| phenotype | Parkinson disease | “Computational association in parkinson's disease SNPs with brain structural and functional alterations.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | SNCA | “SNCA, LRRK2, NURR1, ATP13A2, GSK3B, Parkin, PINK1, DJ-1, and UCHL1are the major genes involved and play a crucial role in the regulatory mechanisms and progression of PD.” | 0.98 | hgnc_dict_v1 |
| gene | LRRK2 | “SNCA, LRRK2, NURR1, ATP13A2, GSK3B, Parkin, PINK1, DJ-1, and UCHL1are the major genes involved and play a crucial role in the regulatory mechanisms and progression of PD.” | 0.98 | hgnc_dict_v1 |
Gene Signals and SNPs Associated with Parkinson's Disease: A Nutrigenomics and Computational Prospective Insights.
PMID 37858629 | DOI 10.1016/j.neuroscience.2023.10.007 · Neuroscience · 2023 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ATP13A2 | “Multigenetic associations of the following genetic alterations in the genes of SNCA, LRRK2, UCHL1, PARK2,PINK1, DJ-1, and ATP13A2 have been reported with the familial and de novo genetic origins of PD.” | 0.98 | hgnc_dict_v1 |
| phenotype | Parkinson disease | “Gene Signals and SNPs Associated with Parkinson's Disease: A Nutrigenomics and Computational Prospective Insights.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | SNCA | “Multigenetic associations of the following genetic alterations in the genes of SNCA, LRRK2, UCHL1, PARK2,PINK1, DJ-1, and ATP13A2 have been reported with the familial and de novo genetic origins of PD.” | 0.98 | hgnc_dict_v1 |
| gene | LRRK2 | “Multigenetic associations of the following genetic alterations in the genes of SNCA, LRRK2, UCHL1, PARK2,PINK1, DJ-1, and ATP13A2 have been reported with the familial and de novo genetic origins of PD.” | 0.98 | hgnc_dict_v1 |
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.
PMID 30833663 | PMCID PMC6399448 | DOI 10.1038/s41598-019-40102-x · Scientific reports · 2019 · 20 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | ATP13A2 | “These variants included loss of function and missense changes in 18 genes that were never previously linked to PD (NOTCH4, BCOR, ITM2B, HRH4, CELSR1, SNAP91, FAM174A, BSN, SPG7, MAGI2, HEPHL1, EPRS, PUM1, CLSTN1, PLCB3, CLSTN3, DNAJB9 and NEFH) and 2 genes that were previously associated with PD (EIF4G1 and ATP13A2).” | 0.98 | hgnc_dict_v1 |
| phenotype | Parkinson disease | “Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | NOTCH4 | “These variants included loss of function and missense changes in 18 genes that were never previously linked to PD (NOTCH4, BCOR, ITM2B, HRH4, CELSR1, SNAP91, FAM174A, BSN, SPG7, MAGI2, HEPHL1, EPRS, PUM1, CLSTN1, PLCB3, CLSTN3, DNAJB9 and NEFH) and 2 genes that were previously associated with PD (EIF4G1 and ATP13A2).” | 0.98 | hgnc_dict_v1 |
| gene | BCOR | “These variants included loss of function and missense changes in 18 genes that were never previously linked to PD (NOTCH4, BCOR, ITM2B, HRH4, CELSR1, SNAP91, FAM174A, BSN, SPG7, MAGI2, HEPHL1, EPRS, PUM1, CLSTN1, PLCB3, CLSTN3, DNAJB9 and NEFH) and 2 genes that were previously associated with PD (EIF4G1 and ATP13A2).” | 0.98 | hgnc_dict_v1 |