PD
MCID: PRK002

Parkinson's Disease malady

Summaries for Parkinson's Disease

Sources:
6Disease Ontology, 23MedlinePlus, 31NINDS, 15GeneReviews, 44Wikipedia, 33OMIM, 22MalaCards
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MedlinePlus: Parkinson's disease is a disorder that affects nerve cells, or neurons, in a part of the brain that controls muscle movement. in parkinson's, neurons that make a chemical called dopamine die or do not work properly. dopamine normally sends signals that help coordinate your movements. no one knows what damages these cells. symptoms of parkinson's disease may include trembling of hands, arms, legs, jaw and face stiffness of the arms, legs and trunk slowness of movement poor balance and coordination as symptoms get worse, people with the disease may have trouble walking, talking or doing simple tasks. they may also have problems such as depression, sleep problems or trouble chewing, swallowing or speaking. parkinson's usually begins around age 60, but it can start earlier. it is more common in men than in women. there is no cure for parkinson's disease. a variety of medicines sometimes help symptoms dramatically.23

MalaCards: Parkinson's Disease, also known as parkinson disease, is related to neuronitis and carcinoma. An important gene associated with Parkinson's Disease is LRRK2 (leucine-rich repeat kinase 2), and among its related pathways are Metabolic pathways and Parkinsons disease. The drugs bromocriptine and pergolide and the compounds lipid and estrogen have been mentioned in the context of this disorder. Affiliated tissues include brain, skin and liver, and related mouse phenotypes are homeostasis/metabolism and behavior/neurological.

Disease Ontology: A neurodegenerative disease that has material basis in degeneration of the central nervous system that often impairs the sufferer's motor skills, speech, and other functions.6

NINDS: Parkinson's disease (PD) belongs to a group of conditions called motor system disorders, which are the result of the loss of dopamine-producing brain cells. The four primary symptoms of PD are tremor, or trembling in hands, arms, legs, jaw, and face; rigidity, or stiffness of the limbs and trunk; bradykinesia, or slowness of movement; and postural instability, or impaired balance and coordination. As these symptoms become more pronounced, patients may have difficulty walking, talking, or completing other simple tasks. PD usually affects people over the age of 50.31

Genetics Home Reference: Parkinson disease is a progressive disorder of the nervous system. The disorder affects several regions of the brain, especially an area called the substantia nigra that controls balance and movement.17

Wikipedia: Parkinson\'s disease (also known as Parkinson disease, Parkinson\'s, idiopathic parkinsonism, primary...44 more...

OMIM: 168600

GeneReviews summary for parkinson-overview

Aliases & Descriptions for Parkinson's Disease

Sources:
6Disease Ontology, 17Genetics Home Reference, 31NINDS, 23MedlinePlus, 43UMLS, 7diseasecard, 15GeneReviews, 16GeneTests, 33OMIM, 32Novoseek , 8DISEASES, 40SNOMED-CT, 19ICD9CM, 27NCIt, 24MeSH
See all sources

Aliases & Descriptions:

parkinson's disease 6 17 31 23
parkinson disease 7 15 16 17 33 32 43
lewy body disease 17 43
parkinson's disease nos (disorder) 6
parkinson disease, mitochondrial 16
parkinson's disease (disorder) 6
parkinson's disease nos 6
primary parkinsonism 17
parkinsons disease 8
paralysis agitans 6
pd 17

Related Diseases for Parkinson's Disease

Sources:
13GeneCards, 14GeneDecks
See all sources

Disease types for parkinson's disease family:

parkinson disease type 3 parkinson disease type 9
parkinson disease 10 parkinson disease-16
parkinson disease 12 parkinson disease 11
parkinson disease 5 parkinson disease 4
parkinson disease 1 parkinson disease 14

Diseases related to parkinson's disease by text searches and GeneDecks gene sharing:

(show top 50)    (show all 968)
idRelated DiseaseScoreTop Affiliating Genes
1neuronitis136.1ZNF746, PIK3CA, PINK1, PIEZO1, PIK3CG, LRP1
2carcinoma124.5PIK3CA, PIR, PIK3CG, LRP1, SH3GLB1, NCL
3alzheimer's disease123.4PIK3CA, PINK1, PIEZO1, PIK3CG, LRP1, NCL
4prostatitis102.0PIK3CA, PINK1, PIK3CG, LRP1, SH3GLB1, NCL
5pancreatitis93.5PIK3CA, PIK3CG, LRP1, SH3GLB1, NCL, RET
6leukemia93.2PIK3CA, PIR, PIK3CG, LRP1, NCL, NCOA1
7cerebritis87.9PIK3CG, LRP1, CNR1, CNTF, SERPINA1, SERPINA3
8neuroblastoma84.2PIK3CA, PIK3CG, LRP1, NCL, NCOA1, RET
9huntington's disease82.2CNR1, CNTF, SERPINA3, VIM, NAT2, VDAC1
10adenocarcinoma80.6PIK3CA, PIK3CG, LRP1, SH3GLB1, NCL, NCOA1
11retinitis79.4PIK3CA, PIK3CG, LRP1, CNR1, CNTF, RB1
12dementia78.8PINK1, PIK3CG, LRP1, SERPINF1, SERPINA1, SERPINA3
13neurodegeneration78.5ZNF746, PINK1, PIK3CG, LRP1, NCL, CNR1
14thyroiditis76.0PIK3CA, PIK3CG, LRP1, NCOA1, RET, RB1
15hepatocellular carcinoma75.8PIK3CA, PIK3CG, NCL, RET, CNR1, VPS35
16melanoma75.1PIK3CA, PIR, PIK3CG, LRP1, NCL, RET
17hypoxia74.8PIK3CA, PIK3CG, LRP1, NCOA1, RET, RB1
18ischemia73.9PIK3CA, PIK3CG, CNR1, CNTF, SERPINF1, SERPINA1
19cholesterol73.5PIK3CA, PIK3CG, LRP1, NCOA1, CNR1, CNTNAP4
20neurodegenerative disease71.4PINK1, PIK3CG, LRP1, CNR1, CNTF, SERPINF1
21arthritis68.9PIK3CG, LRP1, CNR1, CNTF, RB1, SERPINA1
22hypertension67.2PIK3CG, LRP1, RET, CNNM2, CNR1, GCH1
23diabetes mellitus66.1PIK3CA, PIK3CG, RET, CNR1, SERPINA1, SERPINA3
24ovarian cancer66.0PIK3CA, PIK3CG, LRP1, NCOA1, RB1, NBN
25lateral sclerosis65.9ZNF746, CNR1, CNTF, BSG, VEGFA, VDAC2
26multiple sclerosis65.7PINK1, LRP1, CNR1, CNTF, NBN, VIM
27amyotrophic lateral sclerosis65.4ZNF746, CNR1, CNTF, BSG, VEGFA, VDAC2
28gastric cancer64.9PIK3CA, PIK3CG, NCL, RB1, SEMA5A, SERPINA1
29obesity64.3PIK3CA, PIK3CG, LRP1, CNR1, CNTF, SERPINF1
30tuberculosis63.6PIK3CG, CNNM2, SFPQ, GCH1, RB1, SERPINA1
31esophagitis63.6PIK3CA, PIK3CG, RET, CNR1, RB1, NBN
32malaria63.1LRP1, NCL, WBSCR22, CNNM2, CNTF, VPS35
33cervicitis61.5PIK3CA, PIK3CG, NCL, RET, CNR1, GCH1
34rheumatoid arthritis61.5PIK3CG, LRP1, CNR1, CNTF, RB1, SERPINA1
35fibrosis59.1PIK3CA, PIK3CG, LRP1, CNR1, SERPINA1, SERPINA3
36ataxia59.1PIK3CA, PIK3CG, LRP1, NBN, VIM, VIP
37hepatitis b58.9PIK3CA, PIK3CG, RB1, SEMA4D, SERPINA1, VIP
38neuropathy58.7CNR1, CNTF, SERPINF1, VIM, VIP, VEGFA
39atherosclerosis58.6PIK3CG, LRP1, CNR1, GCH1, SERPINF1, SERPINA1
40anemia56.9SFPQ, SFXN2, RB1, NBN, VEGFA, VDR
41asthma56.2PIK3CA, PIK3CG, LRP1, CNR1, SERPINA1, SERPINA3
42blindness55.7PIK3CG, CNR1, CNTF, SERPINF1, VIP, VEGFA
43bipolar disorder55.6CNR1, GCH1, VIP, PAWR, PAH, BDNF
44myeloma53.5PIK3CA, PIK3CG, LRP1, CNTF, RB1, NAT1
45pneumonia53.4CNNM2, GCH1, SERPINA1, VIM, BSG, VEGFA
46myeloid leukemia53.4PIK3CA, PIR, PIK3CG, NCL, RB1, NBN
47squamous cell carcinoma52.7PIK3CA, NCL, RB1, NBN, SEMA4D, SERPINF1
48down syndrome52.6NCL, RET, CNR1, SERPINA3, VIP, VEGFA
49lung carcinoma52.3PIK3CA, PIK3CG, RB1, NBN, SERPINF1, SERPINA1
50multiple system atrophy52.1SEPT8, SERPINA3, PARK7, PARK2, BDNF, CHAT

Graphical network of the top 20 diseases related to parkinson's disease:



Graphical network of diseases related to parkinson's disease

Clinical Features for Parkinson's Disease

Sources:
33OMIM
See all sources
Clinical features from OMIM: 168600

Drugs & Therapeutics for Parkinson's Disease

Sources:
4CenterWatch, 29NIH Clinical Center, 5ClinicalTrials, 21LifeMap Discovery™, 43UMLS, 28NDF-RT
See all sources

Approved drugs:

Search CenterWatch for parkinson's disease

Drug clinical trials:

Search ClinicalTrials for parkinson's disease

Search NIH Clinical Center for parkinson's disease

Search CenterWatch for parkinson's disease

Inferred drug relations via UMLS/NDF-RT:

43 28 amantadine, amantadine hydrochloride, benztropine, benztropine mesylate, biperiden, biperiden hydrochloride, biperiden lactate, bromocriptine, bromocriptine mesylate, cabergoline, carbidopa, entacapone, levodopa, pergolide, pergolide mesylate, pramipexole, pramipexole dihydrochloride, ropinirole, ropinirole hydrochloride, selegiline, selegiline hydrochloride, tolcapone, trihexyphenidyl, trihexyphenidyl hydrochloride

Cell-based therapeutics:


LifeMap Discovery
The database of embryonic development, stem cell research and regenerative medicine

Genetic Tests for Parkinson's Disease

Sources:
16GeneTests
See all sources

Genetic tests related to parkinson's disease:

id Genetic test Affiliating Genes
1 Parkinson's Disease
clinical/research
PINK1, VPS35, PARK7, PARK2, PARK4, UCHL1, FBXO7, HTRA2, NR4A2, SNCAIP (show all 14)

SNCA, RNR1, LRRK2, MT-TT

Anatomical Context for Parkinson's Disease

Sources:
21LifeMap Discovery™, 22MalaCards
See all sources

MalaCards organs/tissues related to parkinson's disease:

22
Brain, Skin, Liver, Lung, Bone marrow, Whole blood, Cortex, Cerebellum, Skeletal muscle, Small intestine, Adrenal gland, Prostate, Monocytes, Nk cells, T cells, B cells, Endothelial, Fetal brain, Prefrontal cortex, Globus pallidus, Olfactory bulb, Thalamus, Hypothalamus, Subthalamic nucleus, Caudate nucleus, Amygdala, Pons, Medulla oblongata, Cardiac myocytes, Fetal liver, Fetal lung, Adrenal cortex

LifeMap Discovery
The database of embryonic development, stem cell research and regenerative medicine

Embryonic and adult cells/anatomical compartments related to parkinson's disease:
id Organ / Tissue -> Anatomical Compartment -> Cell Relevance
1 Brain -> Substantia Nigra  Affected by disease

Phenotypes for genes affiliated with Parkinson's Disease

Sources:
25MGI
See all sources

MGI Mouse Phenotypes related to parkinson's disease:

25 (show all 30)
idDescriptionMGI Source AccessionScoreTop Affiliating Genes
1homeostasis/metabolism phenotypeMP:000537651.6PIK3CA, PINK1, PIK3CG, LRP1, NCOA1, RET
2behavior/neurological phenotypeMP:000538645.8PIK3CA, PINK1, LRP1, NCOA1, CNR1, CNTF
3nervous system phenotypeMP:000363145.2LRP1, RFX4, NCOA1, CNR1, CNTF, RB1
4mortality/agingMP:001076845.1PIK3CA, LRP1, RFX4, PDCD2, RET, CNR1
5growth/size phenotypeMP:000537843.6PIK3CA, PINK1, PIR, PIK3CG, LRP1, NCOA1
6cellular phenotypeMP:000538442.7PIK3CA, PINK1, PIK3CG, SH3GLB1, RET, CNR1
7cardiovascular system phenotypeMP:000538533.6PIK3CA, PIK3CG, LRP1, RET, RB1, SEMA4D
8immune system phenotypeMP:000538728.0PINK1, LRP1, NCOA1, CNTF, NBN, VIM
9normal phenotypeMP:000287326.3LRP1, RET, SEPT6, SEMA5A, VIP, NAT1
10integument phenotypeMP:001077126.0PIK3CG, NCOA1, CNR1, RB1, LMX1A, LMX1B
11reproductive system phenotypeMP:000538925.5PIK3CA, NCOA1, RET, NBN, SERPINF1, SEPT4
12muscle phenotypeMP:000536925.2PIK3CA, PIK3CG, LRP1, RET, CNTF, RB1
13vision/eye phenotypeMP:000539124.2PIK3CA, RB1, SERPINF1, SEMA5A, VIM, NAT1
14hematopoietic system phenotypeMP:000539722.1CNTF, NBN, SEMA4D, SEPT5, BST1, BNIP3
15embryogenesis phenotypeMP:000538021.1PIK3CA, PIR, RFX4, NCOA1, PDCD2, RET
16renal/urinary system phenotypeMP:000536720.8NCOA1, RET, SEMA4D, LMX1B, BMP4, PAH
17skeleton phenotypeMP:000539020.7PIK3CG, LRP1, NCOA1, CNR1, RB1, VEGFA
18no phenotypic analysisMP:000301220.6PINK1, RET, CNR1, RB1, SEMA5A, VEGFA
19digestive/alimentary phenotypeMP:000538120.0RET, RB1, SERPINF1, VEGFA, VDR, MYC
20liver/biliary system phenotypeMP:000537018.5VEGFA, BMP4, LIF, ZFPM1, CHKA, CHRM3
21endocrine/exocrine gland phenotypeMP:000537918.4PINK1, NCOA1, RET, NBN, PARL, PANK2
22adipose tissue phenotypeMP:000537518.1PIK3CA, LRP1, CNR1, RB1, MYC, RAI1
23tumorigenesisMP:000200617.5PIK3CA, RET, RB1, NBN, MYC, RAB25
24respiratory system phenotypeMP:000538817.2RET, VDAC3, RAI1, LIF, PARK2, PARL
25hearing/vestibular/ear phenotypeMP:000537716.9RB1, VDR, LMX1A, MYC, BMP4, PARP1
26limbs/digits/tail phenotypeMP:000537116.1RET, RB1, VEGFA, VDR, VCAN, LMX1A
27craniofacial phenotypeMP:000538215.4NBN, LMX1A, LMX1B, BMP4, RAI1, PAH
28pigmentation phenotypeMP:000118614.8RB1, SERPINF1, LMX1A, MYC, RAC1, PAH
29other phenotypeMP:000539514.4CNR1, VPS35, ATP7B, CD40LG, FN1, GSK3A
30taste/olfaction phenotypeMP:000539413.3CNR1, LMX1B, BDNF, FYN, MKKS, MAPT

Publications for genes affiliated with Parkinson's Disease

Sources:
35PubMed
See all sources

Articles related to parkinson's disease:

(show top 50)    (show all 2730)
idTitleAuthorsYearAffiliating Genes
1Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. (21782285)Sharma M.... KrA1ger R.2011SPR
2Genetic variation in I+-synuclein kinases (CK-2I^ and G RK-5) and risk of Parkinson's disease. (21514207)GarcA-a-Gorostiaga I.... Infante J.2011CSNK2B, XCR1
3ATP13A2 G2236A variant is rare in patients with early -onset Parkinson's disease and familial Parkinson's disease from Mainland China . (20036179)Mao X.Y.... Zhang Z.J.2010ATP13A2
4alpha-Synuclein multiplication analysis in Italian fa milial Parkinson disease. (19833540)Sironi F.... Goldwurm S.2010SNCA
5FGF20 rs12720208 SNP and microRNA-433 variation: no a ssociation with Parkinson's disease in Spanish patients. (20471450)de Mena L.... Alvarez V.2010FGF20, MIR433
6Homology modeling of adenosine A2A receptor and molec ular docking for exploration of appropriate potent antagonists for treatment of Parkinson's disease. (20021407)Singh V.... Somvanshi P.2009ADORA2A
7Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. (19286695)Neumann J.... Wood N.W.2009GBA
8Is there an association between the level of high-sen sitivity C-reactive protein and idiopathic Parkinson's disease? A comparison of Parkinson's disease patients, disease controls and healthy individuals. (19521085)Song I.U.... Lee K.S.2009CRP
9Expression of Cbl-interacting protein of 85 kDa in MPTP mouse model of Parkinson's disease and 1-methyl-4-phenyl-pyridinium ion-treated dopaminergic SH-SY5Y cells. (18535749)Bian M.... Huang F.2008SH3KBP1
10Etiology and pathophysiology of frontotemporal dementia, Parkinson disease and Alzheimer disease: lessons from genetic studies. (18322368)Wider C.... Wszolek Z.K.2008SORL1
11Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset. (18434642)Gan-Or Z.... Orr-Urtreger A.2008GBA, LRRK2
12Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore. (19015489)Lin C.H.... Wu R.M.2008ATP13A2
13Cerebellar {alpha}-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material. (18606870)Westerlund M.... Galter D.2008SNCA
14Clinical, neuropathological and genotypic variability in SNCA A53T familial Parkinson's disease. Variability in familial Parkinson's disease. (18389263)Markopoulou K.... Chase B.A.2008PARK2
15Apolipoprotein E epsilon4 allele is associated with Parkinson disease risk in a Mexican Mestizo population. (17230455)Lopez M.... Alonso M.E.2007APOE
16PINK1 mutants associated with recessive Parkinson's disease are defective in inhibiting mitochondrial release of cytochrome c. (17707122)Wang H.L.... Yu S.T.2007CASP3, EPHA3, PINK1
17Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants. (17222106)Xiromerisiou G.... Singleton A.B.2007SNCA, LRRK2
18Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts. (17192721)Fung H.C.... Singleton A.B.2006MAPT
19PINK-1 and DJ-1--new genes for autosomal recessive Parkinson's disease. (17017532)Heutink P.2006PARK7, PINK1
20Complement C3c and related protein biomarkers in amyotrophic lateral sclerosis and Parkinson's disease. (16516157)Goldknopf I.L.... Appel S.H.2006C3
21Reversible inhibition of mitochondrial complex I activity following chronic dopaminergic glutathione depletion in vitro: implications for Parkinson's disease. (17023271)Chinta S.J.... Andersen J.K.2006NDUFS4
22Ceruloplasmin and superoxide dismutase (SOD1) in Parkinson's disease: a follow-up study. (16352311)TA^rsdA^ttir G.... JA^hannesson T.2006SOD1, CP
23The role of synphilin-1 in the pathogenesis of Parkinson's disease. (17704840)Zheng R.... Chen S.D.2006SNCA, PARK2, RPS27A
24Pathogenesis of Parkinson's disease: implications from familial Parkinson's disease (16447757)Iwatsubo T.... Kuwahara T.2005SNCA, PARK7, PINK1
25Mitochondrial ND5 mutations in idiopathic Parkinson's disease. (15596151)Parker W.D.... Parks J.K.2005MT-ND5
26Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia. (15108120)Autere J.... Majamaa K.2004MT-ND1
27The potential of GDNF as a treatment for Parkinson's disease. (14697313)Hurelbrink C.B.... Barker R.A.2004GDNF
28Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease (15287506)Hattori N.2004SOD1, NDUFS4, SEPT5
29Differential effects of Parkinson's disease-associated mutations on stability and folding of DJ-1. (14607841)Goerner K.... Kahle P.J.2004PARK7
30Ironing iron out in Parkinson's disease and other neurodegenerative diseases with iron chelators: a lesson from 6-hydroxydopamine and iron chelators, desferal and VK-28. (15105275)Youdim M.B.... Ben Shachar D.2004TH
31Minocycline: neuroprotective mechanisms in Parkinson' s disease. (14965330)Thomas M.... Le W.D.2004NOS2
32Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece. (12752402)Papapetropoulos S.... Papapetropoulos T.2003SNCA
33Muscarinic receptors in basal ganglia in dementia with Lewy bodies, Parkinson's disease and Alzheimer's disease. (12706204)Piggott M.A.... Perry E.K.2003ACHE
34Modifications of plasma and platelet levels of L-DOPA and its direct metabolites during treatment with tolcapone or entacapone in pa tients with Parkinson's disease. (12898346)Blandini F.... Martignoni E.2003COMT
35Association of tau gene polymorphism with Parkinson's disease. (14600827)Zappia M.... Quattrone A.2003MAPT
36PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study. (11920285)DeStefano A.L.... Myers R.H.2002PARK3
37Iron and Parkinson's disease. (11843096)Wolozin B.... Golts N.2002SNCA
38Characterisation of isolated alpha-synuclein filaments from substantia nigra of Parkinson's disease brain. (10998565)Crowther R.A.... Goedert M.2000SNCA
39A panel of epitope-specific antibodies detects protein domains distributed throughout human alpha-synuclein in Lewy bodies of Parkinson's disease. (10679792)Giasson B.I.... Lee V.M.2000SNCA
40The EcoRV genetic polymorphism of human monoamine oxidase type A is not associated with Parkinson's disease and does not modify the effect of smoking on Parkinson's disease. (10643794)Costa-Mallen P.... Costa L.G.2000MAOA
41cDNA microarray to study gene expression of dopaminergic neurodegeneration and neuroprotection in MPTP and 6-hydroxydopamine models: implications for idiopathic Parkinson's disease. (11205134)Mandel S.... Youdim M.2000CYP1A1, TFRC, GDNF
42Long-term doxycycline-controlled expression of human tyrosine hydroxylase after direct adenovirus-mediated gene transfer to a rat model of Parkinson's disease. (10518586)Corti O.... Mallet J.1999TH
43Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group. (9802278)Lucking C.B.... Brice A.1998PARK2
44Genetic polymorphism and Parkinson's disease in Taiwan: study of debrisoquine 4-hydroxylase (CYP2D6). (9667775)Lo H.S.... Yan S.H.1998CYP2D6
45Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease. (9634531)Tassin J.... Brice A.1998PARK2
46Apolipoprotein E genotype in familial Parkinson's disease. The French Parkinson's Disease Genetics Study Group. (9328263)1997APOE
47Amyloid beta-peptide and the dementia of Parkinson's disease. (8914090)Jendroska K.... Daniel S.E.1996APP
48Evaluation of the pro-oxidant and antioxidant actions of L-DOPA and dopamine in vitro: implications for Parkinson's disease. (8845917)Spencer J.P.... Halliwell B.1996SERPINA1
49Parkinson's disease: making the diagnosis, selecting drug therapies. (7926845)Scharre D.W.... Mahler M.E.1994MAOB
50Oxidative stress as a cause of nigral cell death in Parkinson's disease and incidental Lewy body disease. The Royal Kings and Queens Parkinson's Disease Research Group. (1510385)Jenner P.... Marsden C.D.1992CAT, NDUFS4

Expression for genes affiliated with Parkinson's Disease

Sources:
1BioGPS
See all sources
Expression patterns in normal tissues for genes affiliated with Parkinson's Disease

Pathways for genes affiliated with Parkinson's Disease

Sources:
20KEGG, 3Cell Signaling Technology, 38Reactome, 36QIAGEN, 41Thomson Reuters, 10EMD Millipore
See all sources

Pathways related to parkinson's disease according to GeneDecks:

(show top 50)    (show all 236)
idPathwayScoreTop Affiliating Genes
1Metabolic pathways2033.6GCH1, BST1, NAT1, NAT2, PAH, PANK2
2Parkinsons disease2028.0PINK1, SEPT5, VDAC1, VDAC2, VDAC3, PARK7
3Huntingtons disease2026.6VDAC2, VDAC3, CLTA, BDNF, UQCR10, UQCR11
4Neuroscience320.7PINK1, RET, PARK7, PARK2, UCHL3, UBE2K
5Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.3820.3UQCR10, UQCR11, UQCRB, UQCRC1, UQCRC2, UQCRFS1
6Neuroactive ligand-receptor interaction2017.1CNR1, LEP, CHRNA6, CHRNA7, CHRM3, CHRNA4
7p38 Signaling3616.8SEMA5A, BMP4, RAC1, LIF, LIFR, BDNF
8Intracellular Calcium Signaling3616.6SEMA5A, BMP4, LIFR, BDNF, CHRNA6, CHRNA7
9DHA Signaling3616.3SERPINF1, SEMA5A, BMP4, BDNF, BCL2, BCL2L1
10Rho Family GTPases3616.2SEMA5A, VIM, BMP4, RAC1, RAC2, LIF
11Cellular Apoptosis Pathway3616.1SEMA5A, VDAC1, VDAC2, VDAC3, BMP4, PAWR
12PAK Pathway3616.0SEMA5A, BMP4, RAC1, RAC2, LIF, PAK4
13Molecular Mechanisms of Cancer3615.8PIK3CG, RB1, SEMA5A, MYC, BMP4, RAC2
14Akt Signaling3615.5PIK3CG, SEMA5A, BMP4, LIF, LIFR, XCR1
15MAPK Family Pathway3615.5SEMA5A, BMP4, RAC1, RAC2, BDNF, BCL2
16eNOS Signaling3615.4SEMA5A, LIFR, BDNF, CHRNA6, CHRNA7, CHRNA4
17p70S6K Signaling3615.2SEMA5A, BMP4, RAC1, RAC2, BDNF, YWHAH
18Paxillin Interactions3614.9SEMA5A, BMP4, RAC1, LIFR, PAK4, PAK7
19Rac1 Pathway3614.6SEMA5A, BMP4, RAC1, PAK4, PAK7, BDNF
20CREB Pathway3614.6SEMA5A, BMP4, BDNF, FGF13, FGF20, FGF8
21Ras Pathway3614.5SEMA5A, BMP4, RAC2, LIFR, PAK4, PAK7
22Neurotrophin signaling pathway2014.5PIK3CA, PIK3CG, RAC1, BDNF, BCL2, YWHAH
23Pathways in cancer2014.4PIK3CA, PIK3CG, RET, RB1, VEGFA, MYC
24Influenza A2014.4PIK3CA, PIK3CG, VDAC1, CIITA, MX1, JUN
25p53 Mediated Apoptosis3614.3SEMA5A, BMP4, BDNF, BCL2, BAX, FGF13
26Pancreatic Adenocarcinoma3613.9RB1, SEMA5A, BMP4, RAC1, RAC2, LIFR
27PPAR Pathway3613.9NCOA1, SEMA5A, BMP4, MRAS, ITGA8, ITGAX
28PEDF Induced Signaling3613.8SERPINF1, BMP4, LIF, BDNF, BCL2, BCL2L1
29Breast Cancer Regulation by Stathmin13613.8SEMA5A, BMP4, RAC1, RAC2, LIFR, MRAS
30Apoptosis2013.7PIK3CA, PIK3CG, BCL2, BCL2L1, CHP1, BAD
31Protein Stability313.5VCP, PARK2, UCHL1, UCHL3, UBA1, UBE2K
32Ceramide Pathway3613.4BAD, MRAS, JUN, FOS, FOSB, FADD
33Proteolysis_Putative ubiquitin pathway4113.2SEPT5, PARK2, UBA1, UBB, UBE2L3, UBE2L6
34JAK-STAT Pathway3611.8SEMA5A, MYC, BMP4, LIFR, BDNF, BCL2
35GSK3 Signaling3611.0SEMA5A, BMP4, LIFR, BDNF, MRAS, CDH8
36PTEN Pathway369.7SEMA5A, BMP4, RAC1, RAC2, BDNF, MRAS
37CDK5 Pathway369.0BDNF, UBB, UBD, UBC, MRAS, CDK5
38RAR-Gamma-RXR-Alpha Degradation369.0BMP4, LIF, UBB, UBD, UBE3A, UBC
39Remodeling of Adherens Junctions368.1CLTA, UBB, UBD, UBE2J1, UBE2J2, UBE2L3
40WNT Signaling368.1VIM, MYC, RAC1, UBB, UBD, UBC
41SOCS Pathway367.8BMP4, BCL2, BAX, IRS2, INS, INSR
42Huntingtons Disease Pathway367.7UBB, UBD, UBC, GRIN2B, GRM5, IGF1
43p53 Signaling367.5BCL2, UBB, UBD, UBC, BAX, FOS
44SREBP Proteolysis366.5GSK3A, GSK3B, SREBF1, PSMA1, PSMA2, PSMA4
45Immune response Antigen presentation by MHC class I106.1B2M, HSP90AA1, PSMA1, PSMA2, PSMA4, PSMA6
46Parkinsons Disease Pathway366.0PINK1, PARK7, PARK2, UCHL1, UBB, UBD
47Proteasome206.0IFNG, PSMA1, PSMA2, PSMA4, PSMA6, PSMA7
48Estrogen-mediated S-Phase Entry366.0RB1, MYC, CCNE1, CCNE2, ESR1, ESR2
49Immune response_Antigen presentation by MHC class I415.9B2M, HSP90AA1, PSMA1, PSMA2, PSMA6, PSMA7
50Metabolism of mRNA385.8RPS6, EIF4G1, PSMA1, PSMA2, PSMA4, PSMA6

Compounds for genes affiliated with Parkinson's Disease

Sources:
32Novoseek , 42Tocris Bioscience, 34PharmGKB, 9DrugBank, 18HMDB
See all sources

Compounds related to parkinson's disease according to GeneDecks:

(show top 50)    (show all 602)
idCompoundScoreTop Affiliating Genes
1lipid32 36.6PIK3CA, PIK3CG, LRP1, NCL, NCOA1, RET
2estrogen32 28.7NCL, NCOA1, GCH1, SERPINA1, SERPINA3, VIP
3dexamethasone32 42 34 9 9 32.6PIK3CA, LRP1, RB1, SERPINF1, SERPINA3, VIM
4acetylcholine32 9 18 9 29.6CNR1, CNTF, SERPINA3, VIM, VIP, RAC1
5vegf32 25.1PIK3CA, PIK3CG, LRP1, RET, CNTF, SERPINF1
6glutamine32 24.7PIK3CG, NCOA1, VIM, VIP, VDAC1, VDR
7ethanol32 34 9 18 9 27.0SERPINA1, BLVRB, BDNF, BCHE, SDHB, CHKA
8potassium32 9 18 9 24.0PIK3CA, CNTF, SERPINF1, VIP, VDAC1, LIF
9cocaine32 9 9 22.7CNR1, CNTF, VIM, BDNF, BCHE, LEP
10heparin32 9 18 9 22.7PIK3CA, PIK3CG, LRP1, NCL, SERPINF1, SERPINA1
11catecholamine32 18.9RET, CNTF, GCH1, VIM, VIP, BLVRB
12paclitaxel32 34 9 9 21.8PIK3CA, PIK3CG, NCL, RB1, VIM, NAT1
13indomethacin32 9 9 20.6NCOA1, CNR1, VIM, VIP, MYC, BLVRB
14threonine32 18.4PINK1, RET, NBN, PAK4, PARK2, CHRNA7
15progesterone32 42 9 18 9 22.3PIK3CA, NCOA1, CNTF, SFPQ, RB1, SERPINA3
16butyrate32 17.9NCOA1, RET, RB1, VIM, VDR, MYC
17quercetin32 42 9 18 9 21.7PIK3CA, PIK3CG, PARP1, BCL2, BCL2L1, BAD
18phospholipid32 17.6SERPINA1, VDAC1, BLZF1, KCNJ5, CHAT, CHKB
19folate32 17.5GCH1, SERPINA3, VIM, NAT1, NAT2, VDR
20wortmannin32 42 18.0PIK3CA, PIK3CG, RET, CNTF, VIM, RAC1
21vitamin d32 16.3LRP1, NCOA1, VIM, VDR, BGLAP, PAH
22sb 20358032 42 17.2RB1, VIM, BSG, VEGFA, VDR, BNIP3
23mg 13232 42 17.0PIK3CG, VDR, MYC, BLZF1, PARP1, PARK2
24polysaccharide32 15.7SERPINA1, SERPINA3, VDAC1, VCAN, VCP, LIF
25simvastatin32 34 42 9 18 9 20.5VEGFA, RAC1, BGLAP, BCHE, CIITA, CHKA
26prostaglandin32 15.4CNTF, VIM, VIP, LIF, KCNJ5, UCP2
27corticosterone32 18 15.8NCOA1, CNR1, VIP, LIF, BGLAP, BDNF
28atropine32 9 9 16.7VIP, BCHE, CHRNA7, CHRM3, CCK, CCKAR
29pdtc32 14.4PIK3CA, PIK3CG, PARP1, BCL2, BCL2L1, XIAP
30n-ethylmaleimide32 9 9 16.4VDAC1, VCP, MYC, BLZF1, P4HB, CDKN3
31guanidine hydrochloride32 14.3CNTF, SERPINA3, VDAC1, BMP4, BGLAP, CHKB
32bromodeoxyuridine32 14.3PIK3CA, CNTF, RB1, VIM, MYC, BMP4
33anisomycin32 42 9 9 17.2PIK3CG, MYC, BDNF, MTOR, JUN, CDC42
34lithium32 34 9 18 9 18.2BDNF, CDK5, FMR1, GSK3A, GSK3B, GRIA3
35quetiapine32 9 18 9 17.1BDNF, LEP, CHRM3, HTR1A, HTR1B, HTR2A
36citalopram32 34 9 18 9 18.1BDNF, LEP, MAOA, MAOB, HTR1A, HTR2A
37rifampicin32 14.1NCOA1, NAT2, FASLG, IAPP, HP, ESRRB
38colchicine32 9 9 16.0VIM, PARK2, BDNF, CHKA, CHAT, CHKB
39vitamin b1232 13.8SERPINA3, MTRR, MTHFR, MTR, B2M, MPO
401 methyl 4 phenylpyridinium32 13.4PARK2, BDNF, BAD, BAX, MAOA, MAOB
41nicotinamide32 9 9 15.2BST1, PARP1, CIITA, INS, GSR, AOX1
42streptozotocin32 13.1SERPINF1, VIM, BDNF, CHGA, UCP2, CDKN3
43atorvastatin32 34 9 18 9 17.1VEGFA, RAC1, CHKA, CHKB, CD40LG, IL10
44sulforaphane32 12.9PIK3CG, RB1, PARP1, JUN, GSTM1, GSTP1
45herbimycin a32 42 13.9PIK3CG, RET, MYC, FYN, JUN, CD14
46suberoylanilide hydroxamic acid32 12.5MYC, PARP1, BCL2, BCL2L1, BAX, XIAP
47thalidomide32 42 9 9 15.3VEGFA, BCL2L1, XIAP, B2M, CD40LG, ITGB2
488-isoprostane32 11.9LEP, XDH, MPO, INS, IL10, IL6
49n acetylcysteine32 11.7BDNF, CDK5, FOS, APOE, MAPT, SNCA
50cyclophosphamide32 34 9 9 14.1ITGB2, TAC1, NPPB

GO Terms for genes affiliated with Parkinson's Disease

Sources:
12Gene Ontology
See all sources

Cellular components related to parkinson's disease according to GeneDecks:

(show all 19)
idNameGO IDScoreTop Affiliating Genes
1cytoplasmGO:00573739.2ZNF746, PIR, PIK3CG, LRP1, SH3GLB1, PDCD2
2plasma membraneGO:00588634.1PIEZO1, PIK3CG, CNR1, SEMA4D, SEPT5, SEMA5A
3cytosolGO:00582930.1PIK3CA, PINK1, PIK3CG, CNTF, VPS35, GCH1
4mitochondrionGO:00573927.5PINK1, KIAA0391, SEPT4, BSG, VDAC1, VDAC2
5integral to plasma membraneGO:00588722.9LRP1, RET, CNR1, SEMA4D, VAMP1, LIFR
6extracellular regionGO:00557622.9PDDC1, SERPINF1, SERPINA1, SERPINA3, VIP, VEGFA
7mitochondrial inner membraneGO:00574322.8SFXN2, VDAC1, VDAC2, PARL, UQCR10, UQCR11
8extracellular spaceGO:00561517.8CNTF, SEMA4D, SERPINF1, SERPINA1, VEGFA, VCAN
9neuronal cell bodyGO:04302516.9CNTF, CHAT, CHRNA4, UCHL1, MTOR, S100B
10axonGO:03042416.4CNTF, VIM, MYC, PARK7, SDC3, KCNJ6
11mitochondrial respiratory chain complex IGO:00574716.2NDUFA1, NDUFA10, NDUFA11, NDUFA12, NDUFA13, NDUFA2
12perinuclear region of cytoplasmGO:04847116.2PARK2, CHERP, MX1, YWHAZ, UBQLN1, BAG5
13cell junctionGO:03005414.3VAMP1, CHRNA6, CHRNA7, CHRM3, CHRNA4, ATN1
14dendriteGO:03042514.2BNIP3, KCNJ6, CHRM3, CHRNA4, UBE2I, MTOR
15terminal buttonGO:04319512.6GRIA3, GRIA4, GRIK2, GRIK3, GRIK4, GRIK5
16nucleoplasmGO:00565412.3NCOA1, SFPQ, RB1, NBN, VDR, BNIP3
17mitochondrial proton-transporting ATP synthase complexGO:00575312.1ATP5D, ATP5B, ATP5O, ATP5J, ATP5E, ATP5G1
18mitochondrial respiratory chainGO:00574611.8UQCRB, UQCRC1, UQCRH, COX7A2, COX7B, COX7B2
19proteasome complexGO:0005027.1VCP, UBE3A, UBE3C, UBQLN1, HSPB1, PSMA1

Biological processes related to parkinson's disease according to GeneDecks:

(show top 50)    (show all 62)
idNameGO IDScoreTop Affiliating Genes
1small molecule metabolic processGO:04428130.7PIK3CA, PIK3CG, NCOA1, GCH1, BSG, NAT1
2respiratory electron transport chainGO:02290421.2UQCR10, UQCR11, UQCRB, UQCRC1, UQCRC2, UQCRFS1
3synaptic transmissionGO:00726819.8VAMP1, KCNJ6, KCNA4, KCNJ3, KCNJ5, KCNN1
4positive regulation of transcription from RNA polymerase II promoterGO:04594417.3RFX4, NCOA1, RB1, VEGFA, VDR, MYC
5response to drugGO:04249317.0NBN, MYC, BGLAP, PARK7, BDNF, BCHE
6anti-apoptosisGO:00691616.0PIK3CA, SH3GLB1, SEMA4D, BNIP3, PAK7, BDNF
7mitochondrial electron transport, NADH to ubiquinoneGO:00612015.8NDUFA1, NDUFA10, NDUFA2, NDUFA3, NDUFA4, NDUFA5
8xenobiotic metabolic processGO:00680515.7NAT1, NAT2, MTR, MGST1, GSTA4, GSTM1
9axon guidanceGO:00741115.6SEMA4D, SEMA5A, LMX1A, RAC1, RAC2, CLTA
10cell deathGO:00821915.5PINK1, VPS35, BNIP3, PARK7, PARK2, PANK2
11apoptotic processGO:00691515.2PDCD2, NBN, SEPT4, VIM, VDAC1, BNIP3
12nerve growth factor receptor signaling pathwayGO:04801115.1PIK3CA, RAC1, LINGO1, CLTA, UBB, UBC
13negative regulation of neuron apoptotic processGO:04352414.9CNTF, PARK7, PARK2, BDNF, BCL2, BCL2L1
14response to hypoxiaGO:00166614.8SERPINA1, VEGFA, BNIP3, BCL2, LEP, CHRNA7
15positive regulation of cell proliferationGO:00828414.8CNTF, NBN, VIP, VEGFA, MYC, RAB25
16oxidation-reduction processGO:05511414.8UQCRB, UQCRC1, UQCRFS1, UQCRH, SDHA, SDHC
17positive regulation of apoptotic processGO:04306514.2NCOA1, CNR1, SEPT4, BMP4, PAWR, UNC5C
18inflammatory responseGO:00695414.0PIK3CG, SERPINA3, RAC1, PARK7, XCR1, CD14
19cell-cell signalingGO:00726713.9SEMA5A, ITGB2, ISG15, INS, FGF13, FGF20
20negative regulation of apoptotic processGO:04306613.6PIK3CG, VEGFA, MYC, BMP4, BCL2, BCL2L1
21agingGO:00756813.2CNR1, SERPINF1, VDR, MSRA, ATP5G3, JUN
22response to ethanolGO:04547113.1CNR1, BGLAP, BCL2, CHAT, ATP5G3, FYN
23induction of apoptosis by intracellular signalsGO:00862913.0BNIP3, MYC, BCL2, BCL2L1, BAD, BAX
24memoryGO:00761313.0CNR1, CHRNA7, CHAT, S100B, ATP1A3, ITGA8
25response to amphetamineGO:00197512.9GRIN1, GRIN2B, ICAM1, DRD1, DRD2, DRD3
26platelet activationGO:03016812.8PIK3CA, PIK3CG, SERPINA1, VEGFA, RAC1, RAC2
27epidermal growth factor receptor signaling pathwayGO:00717312.7PIK3CA, CLTA, UBB, UBC, BAD, MTOR
28neuron apoptotic processGO:05140212.5RB1, BNIP3, BCL2, BAX, ATN1, CDK5
29virus-host interactionGO:01904812.3RB1, SEPT6, VIM, VDAC1, BNIP3, UBE3A
30neurotransmitter biosynthetic processGO:04213612.3PAH, MAOA, ALDH2, ALDH9A1, NOS1, COMT
31response to estradiol stimulusGO:03235511.3NCOA1, SERPINA1, VDR, BMP4, INSR, IL1B
32cellular nitrogen compound metabolic processGO:0346419.7PAH, MTAP, MTR, QDPR, GSTZ1, MCCC1
33regulation of apoptotic processGO:0429818.4SEPT4, VCP, UBB, UBC, CDK5, IL6
34RNA metabolic processGO:0160707.9PAN2, YWHAZ, UBB, UBC, ATXN2, MAPK14
35mRNA metabolic processGO:0160717.8PAN2, YWHAZ, UBB, UBC, MAPK14, HSPB1
36protein polyubiquitinationGO:0002097.6PARK2, UBB, UBC, UBE3C, HUWE1, RPS27A
37S phase of mitotic cell cycleGO:0000847.1RB1, UBB, UBC, GIGYF2, CUL1, RPS27A
38anaphase-promoting complex-dependent proteasomal ubiquitin-dependent protein catabolic processGO:0311457.1UBB, UBC, UBE2S, CDC27, CUL1, RPS27A
39G1/S transition of mitotic cell cycleGO:0000827.1RB1, BCL2, UBB, UBC, CDKN3, CCNE1
40positive regulation of ubiquitin-protein ligase activity involved in mitotic cell cycleGO:0514377.0UBB, UBC, CDC27, CUL1, RPS27A, SKP1
41regulation of ubiquitin-protein ligase activity involved in mitotic cell cycleGO:0514397.0UBB, UBC, CDC27, CUL1, RPS27A, SKP1
42antigen processing and presentation of peptide antigen via MHC class IGO:0024746.9UBB, UBC, B2M, RPS27A, HFE, PSMA1
43M/G1 transition of mitotic cell cycleGO:0002166.8UBB, RPS27A, PSMA1, PSMA2, PSMA4, PSMA6
44antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependentGO:0024796.8UBB, UBC, B2M, RPS27A, PSMA1, PSMA2
45negative regulation of ubiquitin-protein ligase activity involved in mitotic cell cycleGO:0514366.7UBB, UBC, CDC27, RPS27A, PSMA1, PSMA2
46antigen processing and presentation of exogenous peptide antigen via MHC class IGO:0425906.7UBB, UBC, B2M, RPS27A, PSMA1, PSMA2
47DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrestGO:0069776.7UBB, UBC, MDM2, RPS27A, PSMA1, PSMA2
48cell cycle checkpointGO:0000756.6RB1, UBB, UBC, CDC27, MDM2, CCNE2
49regulation of cellular amino acid metabolic processGO:0065216.5INS, NQO1, PSMA1, PSMA2, PSMA4, PSMA6
50mitotic cell cycleGO:0002785.9RB1, UBB, UBC, CDC27, CCNE1, CCNE2

Molecular functions related to parkinson's disease according to GeneDecks:

(show all 15)
idNameGO IDScoreTop Affiliating Genes
1protein bindingGO:00551546.1ADORA2A, EPHB1, EPHA4, EPHA3, E2F1, HDAC6
2ATP bindingGO:00552420.2PPP2R4, NOD2, NLRP1, PDXK, NDUFA10, NDUFA13
3protein homodimerization activityGO:04280319.0S100B, BAX, CHRNA7, CHKA, BCL2, PAH
4electron carrier activityGO:00905516.3AIFM1, AKR1B1, AKR1A1, GLRX2, GLRX, ALDH2
5NADH dehydrogenase (ubiquinone) activityGO:00813716.0NDUFAF2, NDUFAB1, NDUFA9, NDUFA8, NDUFA7, NDUFA6
6receptor bindingGO:00510215.1CSNK2B, CXCL12, PSPN, TGFB2, GFRA1, NOS2
7enzyme bindingGO:01989914.9NOD2, PPARG, PPP3CA, CYP2E1, CYP2C19, CYP2A6
8drug bindingGO:00814414.5DRD5, DRD4, DRD3, DRD2, DRD1, HMGCS1
9identical protein bindingGO:04280214.5SNCA, PTS, TNF, ESR1, AKT1, GLUL
10iron ion bindingGO:00550614.0CYP17A1, CYCS, CYC1, CYP2D6, CYP2E1, CYP2C19
11growth factor activityGO:00808314.0GH1, TGFB1, HBEGF, EGF, NGF, NRTN
12ubiquitin protein ligase bindingGO:03162513.8NGFR, SNCAIP, CUL2, CUL1, SUMO1, HSPA1B
13cytochrome-c oxidase activityGO:00412913.2COX8A, COX7A2L, COX7A1, COX6B2, COX6C, COX5B
14heme bindingGO:02003713.0CYC1, CYP2D6, CYP2E1, CYP2C19, CYP2B6, CYCS
15threonine-type endopeptidase activityGO:0042989.2PSMB7, PSMA3, PSMA5, PSMB1, PSMB3, PSMB6

Sources for Parkinson's Disease

2CDC
11FMA
18HMDB
19ICD9CM
20KEGG
24MeSH
25MGI
27NCIt
28NDF-RT
31NINDS
32Novoseek
33OMIM
35PubMed
36QIAGEN
43UMLS