ATP13A2, ATPase cation transporting 13A2, 23400

N. diseases: 160; N. variants: 31
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853967
rs137853967
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C1847640
Disease:
KUFOR-RAKEB SYNDROME
0.710 GeneticVariation BEFREE Recently, we identified novel compound heterozygous mutations, c.3176T>G (p.L1059R) and c.3253delC (p.L1085WfsX1088) in ATP13A2 of two siblings affected with KRS. 21542062 2011
dbSNP: rs147277743
rs147277743
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C1847640
Disease:
KUFOR-RAKEB SYNDROME
0.710 GeneticVariation BEFREE The association between idiopathic Parkinson's disease (PD) and the ATP13A2 (PARK9) Ala746Thr variant, associated with Kufor-Rakeb syndrome, is controversial. 23522931 2013
dbSNP: rs147277743
rs147277743
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE The ATP13A2 A746T variant is rare in Han Chinese patients and controls and is not associated with PD susceptibility in this ethnic group. 26000924 2016
dbSNP: rs147277743
rs147277743
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE We suggest that the ATP13A2 Ala746Thr variant is not a common risk factor for PD in the Chinese population in Hong Kong. 23522931 2013
dbSNP: rs147277743
rs147277743
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE The clinical features and 99mTc-TRODAT-1 single photon emission computed tomography (SPECT) image of the patients carrying G1014S and A746T were similar to that of idiopathic PD. 21714071 2011
dbSNP: rs147277743
rs147277743
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE These results suggest that ATP13A2 p.A746T variant is unlikely to play a role as a common risk factor or a pathogenic mutation for PD at least in Japanese. 20976737 2010
dbSNP: rs147277743
rs147277743
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.050 GeneticVariation BEFREE We did not observe a significant association between Ala746Thr and Parkinson's disease in Han Chinese population, even after stratification by age at onset. 20227461 2010
dbSNP: rs121918227
rs121918227
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0752105
Disease:
Parkinsonism, Juvenile
0.010 GeneticVariation BEFREE A novel homozygous missense mutation (Gly504Arg) was identified in one sporadic case from Brazil with juvenile parkinsonism. 17485642 2007
dbSNP: rs12564040
rs12564040
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE The observed heterozygosities of the rs4538475 and rs11107 loci in PD and control groups ranged from 0.460 - 0.481 and 0.410 - 0.441, in BST1, PARK15 respectively, while we detected no heterozygosity at the rs12564040 locus in PARK9. 22490479 2012
dbSNP: rs1373219981
rs1373219981
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0151786
Disease:
Muscle Weakness
0.010 GeneticVariation BEFREE In addition, our study revealed a novel missense mutation in PLA2G6 gene (c.3G > T:p.M1I) in one and half-year-old boy with muscle weakness and neurodevelopmental regression (speech, motor and cognition). 28821231 2017
dbSNP: rs1373219981
rs1373219981
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030552
Disease:
Paresis
0.010 GeneticVariation BEFREE In addition, our study revealed a novel missense mutation in PLA2G6 gene (c.3G > T:p.M1I) in one and half-year-old boy with muscle weakness and neurodevelopmental regression (speech, motor and cognition). 28821231 2017
dbSNP: rs151117874
rs151117874
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE Furthermore, two Italian cases with YOPD without atypical features carried a novel missense mutation (Thr12Met, Gly533Arg) in single heterozygous state. 17485642 2007
dbSNP: rs151181674
rs151181674
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE This study explored the mutations at the Thr12Met and Ala1144Thr gene loci of the ATP13A2 gene in Parkinson's disease patients in the Uygur and Han populations in the Xinjiang province. 25374329 2014
dbSNP: rs2871776
rs2871776
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0814161
Disease:
impaired motor coordination
0.010 GeneticVariation BEFREE ATP13A2 polymorphisms rs4920608 and rs2871776 significantly modified the effects of Mn exposure on impaired motor coordination in elderly (p for interaction=0.029, p=0.041, respectively), also after adjustments for age and gender. 22285144 2012
dbSNP: rs4920608
rs4920608
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0814161
Disease:
impaired motor coordination
0.010 GeneticVariation BEFREE ATP13A2 polymorphisms rs4920608 and rs2871776 significantly modified the effects of Mn exposure on impaired motor coordination in elderly (p for interaction=0.029, p=0.041, respectively), also after adjustments for age and gender. 22285144 2012
dbSNP: rs781734330
rs781734330
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0027819
Disease:
Neuroblastoma
0.010 GeneticVariation BEFREE To this end, we generated a set of melanoma and neuroblastoma cell lines stably overexpressing wild-type (WT), catalytically inactive (D508N) and N-terminal mutants, or shRNA against ATP13A2. 28334751 2017
dbSNP: rs781734330
rs781734330
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C4086165
Disease:
Childhood Neuroblastoma
0.010 GeneticVariation BEFREE To this end, we generated a set of melanoma and neuroblastoma cell lines stably overexpressing wild-type (WT), catalytically inactive (D508N) and N-terminal mutants, or shRNA against ATP13A2. 28334751 2017
dbSNP: rs781734330
rs781734330
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0700095
Disease:
Central neuroblastoma
0.010 GeneticVariation BEFREE To this end, we generated a set of melanoma and neuroblastoma cell lines stably overexpressing wild-type (WT), catalytically inactive (D508N) and N-terminal mutants, or shRNA against ATP13A2. 28334751 2017
dbSNP: rs781734330
rs781734330
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C0025202
Disease:
melanoma
0.010 GeneticVariation BEFREE To this end, we generated a set of melanoma and neuroblastoma cell lines stably overexpressing wild-type (WT), catalytically inactive (D508N) and N-terminal mutants, or shRNA against ATP13A2. 28334751 2017
dbSNP: rs1057519291
rs1057519291
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C4310662
Disease:
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
A 0.800 CausalMutation CLINVAR
dbSNP: rs121918227
rs121918227
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C1847640
Disease:
KUFOR-RAKEB SYNDROME
G 0.800 CausalMutation CLINVAR
dbSNP: rs144701072
rs144701072
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C1847640
Disease:
KUFOR-RAKEB SYNDROME
T 0.800 CausalMutation CLINVAR
dbSNP: rs587777053
rs587777053
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C1847640
Disease:
KUFOR-RAKEB SYNDROME
C 0.800 CausalMutation CLINVAR
dbSNP: rs1057519289
rs1057519289
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C4310662
Disease:
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
A 0.700 CausalMutation CLINVAR
dbSNP: rs1057519290
rs1057519290
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
CUI: C4310662
Disease:
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
G 0.700 CausalMutation CLINVAR