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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Parkinsonism
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Accession:DOID:0080855 term browser browse the term
Definition:A movement disorder that is characterized by disturbances of balance, gait and posture. (DO)
Synonyms:exact_synonym: Autosomal Dominant Juvenile Parkinsonism;   Autosomal Dominant Parkinsonism;   Autosomal Recessive Juvenile Parkinson Disease;   Autosomal Recessive Parkinsonism;   Autosomal Recesssive Juvenile Parkinsonism;   Chromosome 6 Linked Autosomal Recessive Parkinsonism;   EPDF;   Experimental Parkinson Disease;   Experimental Parkinsonism;   Familial Juvenile Parkinsonism;   Familial Parkinson Disease, Autosomal Recessive;   Juvenile Parkinson Disease;   Juvenile Parkinsonism;   Juvenile Parkinsonism, Autosomal Recessive;   MPTP Induced Experimental Parkinsonism;   PDJ;   Parkinsonian Disorders;   Parkinsonian Syndrome;   Parkinsonian disorder;   Ramsay Hunt paralysis syndrome;   autosomal dominant juvenile Parkinson disease;   experimental Parkinson diseases;   parkinsonian diseases;   parkinsonian syndromes
 primary_id: MESH:D020734

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Parkinsonism term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Abat 4-aminobutyrate aminotransferase treatment ISO RGD PMID:22634324 RGD:9588554 NCBI chrNW_004624824:6,112,644...6,202,936
Ensembl chrNW_004624824:6,141,213...6,202,936 		JBrowse link
G Abcc8 ATP binding cassette subfamily C member 8 ISO RGD PMID:15857625 RGD:1598645 NCBI chrNW_004624766:9,018,616...9,092,365
Ensembl chrNW_004624766:9,018,721...9,092,287 		JBrowse link
G Abcc9 ATP binding cassette subfamily C member 9 ISO RGD PMID:15857625 RGD:1598645 NCBI chrNW_004624752:16,792,202...16,926,552
Ensembl chrNW_004624752:16,792,165...16,927,293 		JBrowse link
G Adcyap1 adenylate cyclase activating polypeptide 1 ISO RGD PMID:16888218 RGD:2325295 NCBI chrNW_004624770:11,359,606...11,375,833
Ensembl chrNW_004624770:11,358,286...11,375,813 		JBrowse link
G Aldh1a1 aldehyde dehydrogenase 1 family member A1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25045800 NCBI chrNW_004624811:505,297...563,795
Ensembl chrNW_004624811:505,101...563,855 		JBrowse link
G Aldh1a2 aldehyde dehydrogenase 1 family member A2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25045800 NCBI chrNW_004624781:13,756,469...13,845,253
Ensembl chrNW_004624781:13,756,390...13,845,479 		JBrowse link
G Apaf1 apoptotic peptidase activating factor 1 treatment ISO RGD PMID:11535810 RGD:13503334 NCBI chrNW_004624750:8,835,521...8,940,957
Ensembl chrNW_004624750:8,837,037...8,938,009 		JBrowse link
G Aqp4 aquaporin 4 severity ISO RGD PMID:21255222 RGD:5148006 NCBI chrNW_004624770:5,581,192...5,593,470
Ensembl chrNW_004624770:5,580,808...5,594,628 		JBrowse link
G Atp13a2 ATPase cation transporting 13A2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:23046578 NCBI chrNW_004624764:2,614,541...2,631,972
Ensembl chrNW_004624764:2,614,827...2,631,793 		JBrowse link
G Atp1a3 ATPase Na+/K+ transporting subunit alpha 3 ISO CTD Direct Evidence: marker/mechanism CTD PMID:15260953 NCBI chrNW_004624907:715,109...736,040
Ensembl chrNW_004624907:715,094...736,432 		JBrowse link
G Bad BCL2 associated agonist of cell death ISO RGD PMID:23251488 RGD:10053712 NCBI chrNW_004624767:22,025,721...22,037,283
Ensembl chrNW_004624767:22,026,133...22,037,277 		JBrowse link
G Bdnf brain derived neurotrophic factor treatment ISO RGD PMID:16018990 RGD:8657066 NCBI chrNW_004624766:17,281,882...17,330,601
Ensembl chrNW_004624766:17,279,630...17,330,490 		JBrowse link
G Becn1 beclin 1 treatment ISO RGD PMID:19864570 PMID:25424835 RGD:11558014 RGD:6483312 NCBI chrNW_004624795:1,386,154...1,406,314
Ensembl chrNW_004624795:1,385,756...1,405,714 		JBrowse link
G Casp9 caspase 9 treatment ISO RGD PMID:26612350 RGD:13503344 NCBI chrNW_004624764:1,769,270...1,789,399
Ensembl chrNW_004624764:1,773,455...1,789,423 		JBrowse link
G Cnr1 cannabinoid receptor 1 ISO RGD PMID:19414037 RGD:2314672 NCBI chrNW_004624799:6,100,709...6,126,530
Ensembl chrNW_004624799:6,101,728...6,126,520 		JBrowse link
G Comt catechol-O-methyltransferase ISO RGD PMID:15698633 RGD:2289785 NCBI chrNW_004624747:569,127...588,479
Ensembl chrNW_004624747:581,832...588,333 		JBrowse link
G Csf1r colony stimulating factor 1 receptor ISO ClinVar Annotator: match by term: Parkinsonian disorder ClinVar PMID:25741868 NCBI chrNW_004624774:9,363,156...9,391,939
Ensembl chrNW_004624774:9,363,908...9,391,986 		JBrowse link
G Csf2 colony stimulating factor 2 ISO RGD PMID:21291297 RGD:5131508 NCBI chrNW_004624733:40,039,127...40,041,294
Ensembl chrNW_004624733:40,039,414...40,041,294 		JBrowse link
G Cx3cl1 C-X3-C motif chemokine ligand 1 ISO RGD PMID:19368990 RGD:4891964 NCBI chrNW_004624746:28,677,956...28,688,638
Ensembl chrNW_004624746:28,677,709...28,689,122 		JBrowse link
G Cx3cr1 C-X3-C motif chemokine receptor 1 ISO RGD PMID:19368990 RGD:4891964 NCBI chrNW_004624731:1,705,953...1,719,452
Ensembl chrNW_004624731:1,706,043...1,719,452 		JBrowse link
G Dctn1 dynactin subunit 1 ISO ClinVar Annotator: match by term: Parkinsonian disorder ClinVar PMID:25741868 PMID:28492532 PMID:28518168 PMID:29525180 PMID:32461654 NCBI chrNW_004624749:29,105,310...29,135,124
Ensembl chrNW_004624749:29,115,561...29,137,276 		JBrowse link
G Ddc dopa decarboxylase ISO CTD Direct Evidence: therapeutic CTD PMID:16269145 NCBI chrNW_004624740:3,674,727...3,732,058
Ensembl chrNW_004624740:3,674,609...3,732,676 		JBrowse link
G Drd2 dopamine receptor D2 ISO CTD Direct Evidence: marker/mechanism|therapeutic CTD
RGD		 PMID:9171869 PMID:12476322 PMID:15469457 PMID:22126770 RGD:6907448 NCBI chrNW_004624784:8,828,589...8,906,617
Ensembl chrNW_004624784:8,827,006...8,865,529 		JBrowse link
G Drd3 dopamine receptor D3 ISO RGD PMID:12535962 RGD:1358605 NCBI chrNW_004624731:34,318,733...34,369,111
Ensembl chrNW_004624731:34,319,130...34,363,184 		JBrowse link
G Egfr epidermal growth factor receptor ISO protein:decreased expression:striatum RGD PMID:15857400 RGD:2289955 NCBI chrNW_004624740:584,133...713,205
Ensembl chrNW_004624740:589,606...713,271 		JBrowse link
G En1 engrailed homeobox 1 ISO RGD PMID:17015829 RGD:5687199 NCBI chrNW_004624732:26,333,642...26,338,450
Ensembl chrNW_004624732:26,333,653...26,337,904 		JBrowse link
G En2 engrailed homeobox 2 ISO RGD PMID:17015829 RGD:5687199 NCBI chrNW_004624800:2,440,502...2,446,647
Ensembl chrNW_004624800:2,438,900...2,446,680 		JBrowse link
G Eno2 enolase 2 ISO RGD PMID:17532790 RGD:2293747 NCBI chrNW_004624860:3,553,936...3,561,343
Ensembl chrNW_004624860:3,553,947...3,564,294 		JBrowse link
G Esr1 estrogen receptor 1 ISO RGD PMID:21420980 RGD:8553241 NCBI chrNW_004624785:6,164,507...6,601,302
Ensembl chrNW_004624785:6,164,379...6,601,326 		JBrowse link
G Fgf2 fibroblast growth factor 2 treatment ISO RGD PMID:27228974 RGD:13801017 NCBI chrNW_004624777:3,268,674...3,321,424
Ensembl chrNW_004624777:3,268,953...3,321,145 		JBrowse link
G Fkbp1a FKBP prolyl isomerase 1A ISO mRNA, protein:increased expression:brain RGD PMID:17877381 RGD:2302074 NCBI chrNW_004624741:2,669,909...2,692,959
Ensembl chrNW_004624741:2,666,636...2,692,938 		JBrowse link
G Gapdh glyceraldehyde-3-phosphate dehydrogenase ISO CTD Direct Evidence: marker/mechanism CTD PMID:29886133 NCBI chrNW_004624860:3,257,805...3,261,736
Ensembl chrNW_004624860:3,257,853...3,261,735 		JBrowse link
G Gba1 glucosylceramidase beta 1 severity ISO DNA:missense mutations:cds:multiple (human)
ClinVar Annotator: match by term: Parkinsonian disorder | ClinVar Annotator: match by term: Parkinsonism		 RGD
ClinVar		 PMID:1864608 PMID:1899336 PMID:1972019 PMID:2309702 PMID:2378352 More... RGD:5508426 NCBI chrNW_004624885:2,315,371...2,321,327
Ensembl chrNW_004624885:2,315,142...2,321,327 		JBrowse link
G Gch1 GTP cyclohydrolase 1 treatment ISO RGD PMID:12451130 PMID:15684695 PMID:16708545 PMID:23831692 PMID:25592335 RGD:1580026 RGD:329970292 RGD:401700381 RGD:401700385 RGD:628489 NCBI chrNW_004624731:14,459,164...14,502,485
Ensembl chrNW_004624731:14,459,303...14,500,429 		JBrowse link
G Gdnf glial cell derived neurotrophic factor treatment ISO protein:decreased expression:brain
CTD Direct Evidence: therapeutic		 RGD
CTD		 PMID:9266731 PMID:12213621 PMID:16018990 PMID:21147986 PMID:21865882 More... RGD:405878061 RGD:405878069 RGD:405878071 RGD:5686884 RGD:6218962 RGD:8657066 NCBI chrNW_004624759:17,263,570...17,290,046
Ensembl chrNW_004624759:17,263,969...17,287,723 		JBrowse link
G Gfra1 GDNF family receptor alpha 1 ISO mRNA:altered expression:brain RGD PMID:12210101 PMID:21865882 RGD:6218962 RGD:6218972 NCBI chrNW_004624737:30,325,962...30,526,311
Ensembl chrNW_004624737:30,324,515...30,526,486 		JBrowse link
G Gfra2 GDNF family receptor alpha 2 ISO mRNA:decreased expression:brain RGD PMID:12210101 RGD:6218972 NCBI chrNW_004624758:17,330,401...17,417,435
Ensembl chrNW_004624758:17,330,020...17,417,572 		JBrowse link
G Gja1 gap junction protein alpha 1 treatment ISO RGD PMID:23783886 RGD:8662444 NCBI chrNW_004624798:9,358,996...9,364,413
Ensembl chrNW_004624798:9,359,004...9,364,313 		JBrowse link
G Gnal G protein subunit alpha L ISO RGD PMID:22539851 RGD:13513924 NCBI chrNW_004624770:19,433,614...19,504,759
Ensembl chrNW_004624770:19,433,660...19,504,698 		JBrowse link
G Grm8 glutamate metabotropic receptor 8 ISO RGD PMID:22546615 RGD:6771180 NCBI chrNW_004624783:8,727,563...9,611,933
Ensembl chrNW_004624783:8,737,463...9,611,475 		JBrowse link
G Grn granulin precursor ISO ClinVar Annotator: match by term: Parkinsonian disorder ClinVar NCBI chrNW_004624795:704,066...708,721
Ensembl chrNW_004624795:704,252...707,165 		JBrowse link
G Gsk3a glycogen synthase kinase 3 alpha ISO protein:decreased expression:striatum RGD PMID:18805403 RGD:10401814 NCBI chrNW_004624907:511,919...522,106
Ensembl chrNW_004624907:511,889...522,168 		JBrowse link
G Gsr glutathione-disulfide reductase treatment ISO CTD Direct Evidence: therapeutic CTD
RGD		 PMID:20951685 PMID:22721943 RGD:5128840 NCBI chrNW_004624780:13,440,269...13,497,435
Ensembl chrNW_004624780:13,440,235...13,496,535 		JBrowse link
G Hmox1 heme oxygenase 1 treatment ISO RGD PMID:24169105 RGD:10755712 NCBI chrNW_004624750:341,699...346,005
Ensembl chrNW_004624750:342,146...345,887 		JBrowse link
G Hspa9 heat shock protein family A (Hsp70) member 9 ISO protein:decreased expression:striatum RGD PMID:21542017 RGD:6784518 NCBI chrNW_004624743:31,324,085...31,345,681
Ensembl chrNW_004624743:31,324,085...31,345,695 		JBrowse link
G Htra2 HtrA serine peptidase 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:26558463 NCBI chrNW_004624749:28,980,375...28,983,719
Ensembl chrNW_004624749:28,980,362...28,983,869 		JBrowse link
G Il1b interleukin 1 beta ISO protein:increased expression:hypothalamus RGD PMID:17520785 RGD:1626658 NCBI chrNW_004624749:12,852,128...12,858,478
Ensembl chrNW_004624749:12,852,021...12,858,760 		JBrowse link
G Kcnj11 potassium inwardly rectifying channel subfamily J member 11 ISO mRNA, protein:increased expression:prefrontal cortex, striatum, hippocampus (rat) RGD PMID:15857625 RGD:1598645 NCBI chrNW_004624766:9,012,166...9,015,269
Ensembl chrNW_004624766:9,013,225...9,014,397 		JBrowse link
G Kcnj8 potassium inwardly rectifying channel subfamily J member 8 ISO mRNA, protein:increased expression:striatum, hippocampus (rat) RGD PMID:15857625 RGD:1598645 NCBI chrNW_004624752:16,939,289...16,945,692
Ensembl chrNW_004624752:16,939,384...16,946,723 		JBrowse link
G LOC101698338 E3 SUMO-protein ligase RanBP2 severity ISO RGD PMID:22821000 RGD:9835348 NCBI chrNW_004624749:11,862,670...11,923,291
Ensembl chrNW_004624749:11,862,760...11,923,958 		JBrowse link
G LOC101707509 cytochrome P450 1A1 ISO mRNA:decreased expression:striatum RGD PMID:18374908 RGD:5147675 NCBI chrNW_004627988:7...1,323 JBrowse link
G Lrrk2 leucine rich repeat kinase 2 ISO CTD Direct Evidence: marker/mechanism RGD
CTD		 PMID:20729864 PMID:23046578 PMID:25017139 PMID:26558463 RGD:5508414 NCBI chrNW_004624778:106,594...279,325
Ensembl chrNW_004624778:108,761...279,230 		JBrowse link
G Lyn LYN proto-oncogene, Src family tyrosine kinase ISO RGD PMID:16529858 RGD:1581410 NCBI chrNW_004624886:4,029,318...4,168,797
Ensembl chrNW_004624886:4,027,178...4,168,902 		JBrowse link
G Manf mesencephalic astrocyte derived neurotrophic factor ISO RGD PMID:19641128 RGD:2325813 NCBI chrNW_004624730:5,165,169...5,168,240
Ensembl chrNW_004624730:5,165,200...5,168,240 		JBrowse link
G Mapk8 mitogen-activated protein kinase 8 treatment ISO RGD PMID:20581854 RGD:401965387 NCBI chrNW_004624928:1,442,216...1,494,275
Ensembl chrNW_004624928:1,439,146...1,494,266 		JBrowse link
G Mapt microtubule associated protein tau treatment ISO ClinVar Annotator: match by term: Parkinsonian disorder RGD
ClinVar		 PMID:27228974 RGD:13801017 NCBI chrNW_004624849:2,320,887...2,421,099 JBrowse link
G Mmp3 matrix metallopeptidase 3 treatment ISO RGD PMID:22498097 RGD:8693688 NCBI chrNW_004624878:39,282...47,386
Ensembl chrNW_004624878:39,358...47,075 		JBrowse link
G Mmp9 matrix metallopeptidase 9 treatment ISO RGD PMID:15075439 RGD:13204850 NCBI chrNW_004624790:8,584,399...8,591,763
Ensembl chrNW_004624790:8,583,457...8,591,713 		JBrowse link
G Mre11 MRE11 homolog, double strand break repair nuclease ISO ClinVar Annotator: match by term: Parkinsonism ClinVar PMID:25741868 PMID:26467025 PMID:26878173 PMID:26898890 PMID:27878467 More... NCBI chrNW_004624735:39,095,559...39,153,936
Ensembl chrNW_004624735:39,092,781...39,153,920 		JBrowse link
G Mtor mechanistic target of rapamycin kinase treatment ISO RGD PMID:20089925 RGD:10040992 NCBI chrNW_004624818:1,570,155...1,698,264
Ensembl chrNW_004624818:1,570,276...1,698,259 		JBrowse link
G Ndufs3 NADH:ubiquinone oxidoreductase core subunit S3 ISO RGD PMID:20403401 RGD:13824972 NCBI chrNW_004624767:1,238,953...1,243,945
Ensembl chrNW_004624767:1,237,261...1,244,031 		JBrowse link
G Nfkb2 nuclear factor kappa B subunit 2 ISO RGD PMID:18534259 RGD:2302392 NCBI chrNW_004624831:1,804,050...1,810,309
Ensembl chrNW_004624831:1,803,917...1,810,187 		JBrowse link
G Ngf nerve growth factor treatment ISO CTD Direct Evidence: therapeutic CTD
RGD		 PMID:19694610 PMID:20581854 RGD:401965387 NCBI chrNW_004624772:11,009,765...11,070,050
Ensembl chrNW_004624772:11,010,845...11,070,017 		JBrowse link
G Ngfr nerve growth factor receptor treatment ISO RGD PMID:20581854 RGD:401965387 NCBI chrNW_004624795:5,623,686...5,639,545
Ensembl chrNW_004624795:5,623,700...5,639,655 		JBrowse link
G Nos1 nitric oxide synthase 1 ISO RGD PMID:23967645 RGD:7257596 NCBI chrNW_004624747:15,940,614...16,118,051
Ensembl chrNW_004624747:16,003,969...16,113,165 		JBrowse link
G Nr4a2 nuclear receptor subfamily 4 group A member 2 treatment ISO RGD PMID:31408200 RGD:124713575 NCBI chrNW_004624732:9,572,160...9,589,624
Ensembl chrNW_004624732:9,581,779...9,589,942 		JBrowse link
G Ntrk1 neurotrophic receptor tyrosine kinase 1 treatment ISO RGD PMID:20581854 RGD:401965387 NCBI chrNW_004624885:1,989,027...2,005,474
Ensembl chrNW_004624885:1,989,138...2,005,577 		JBrowse link
G Pacrg parkin coregulated ISO ClinVar Annotator: match by term: Juvenile parkinsonism ClinVar NCBI chrNW_004624855:99,475...430,105 JBrowse link
G Park7 Parkinsonism associated deglycase treatment ISO CTD Direct Evidence: marker/mechanism
protein:decreased expression:brain		 RGD
CTD		 PMID:16860563 PMID:18373560 PMID:22041943 PMID:22710069 PMID:23046578 More... RGD:13210569 RGD:13462067 RGD:13463452 RGD:13463458 RGD:1601076 NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Parp1 poly(ADP-ribose) polymerase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:17640816 NCBI chrNW_004624807:446,662...478,571
Ensembl chrNW_004624807:446,647...479,069 		JBrowse link
G Pde1b phosphodiesterase 1B ISO RGD PMID:15305867 RGD:2312524 NCBI chrNW_004624904:2,580,055...2,607,961
Ensembl chrNW_004624904:2,580,322...2,607,961 		JBrowse link
G Pdgfrb platelet derived growth factor receptor beta ISO ClinVar Annotator: match by term: Parkinsonian disorder ClinVar PMID:25741868 NCBI chrNW_004624774:9,432,765...9,469,690
Ensembl chrNW_004624774:9,432,541...9,469,881 		JBrowse link
G Pdyn prodynorphin disease_progression ISO CTD Direct Evidence: marker/mechanism
mRNA:increased expression:striatum		 CTD
RGD		 PMID:9930741 PMID:26113400 RGD:401851054 NCBI chrNW_004624741:3,239,101...3,253,507
Ensembl chrNW_004624741:3,237,942...3,253,503 		JBrowse link
G Pink1 PTEN induced kinase 1 ISO CTD Direct Evidence: marker/mechanism CTD
RGD		 PMID:11254447 PMID:15349871 PMID:23046578 PMID:24441527 PMID:24792327 More... RGD:13210569 NCBI chrNW_004624764:5,656,207...5,671,260
Ensembl chrNW_004624764:5,656,229...5,671,260 		JBrowse link
G Pnoc prepronociceptin ISO CTD Direct Evidence: marker/mechanism CTD PMID:26687234 NCBI chrNW_004624758:23,007,530...23,026,962
Ensembl chrNW_004624758:23,007,573...23,028,704 		JBrowse link
G Polg DNA polymerase gamma, catalytic subunit ISO CTD Direct Evidence: marker/mechanism CTD PMID:17923349 NCBI chrNW_004624768:16,493,123...16,509,747
Ensembl chrNW_004624768:16,491,555...16,509,900 		JBrowse link
G Ppargc1a PPARG coactivator 1 alpha ISO RGD PMID:21376232 PMID:22040668 PMID:22246294 RGD:6484262 RGD:6484267 RGD:6484271 NCBI chrNW_004624755:7,826,219...8,460,746
Ensembl chrNW_004624755:8,375,596...8,465,297 		JBrowse link
G Prkcd protein kinase C delta ISO CTD Direct Evidence: therapeutic CTD PMID:15681813 NCBI chrNW_004624822:4,035,819...4,062,907
Ensembl chrNW_004624822:4,033,130...4,059,555 		JBrowse link
G Prkn parkin RBR E3 ubiquitin protein ligase ISO ClinVar Annotator: match by term: Juvenile parkinsonism ClinVar PMID:10072423 PMID:10824074 PMID:11179010 PMID:11558785 PMID:11889248 More... NCBI chrNW_004624855:430,148...1,992,121
Ensembl chrNW_004624855:430,260...1,989,747 		JBrowse link
G Prkra protein activator of interferon induced protein kinase EIF2AK2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:18243799 NCBI chrNW_004624844:410,461...424,833
Ensembl chrNW_004624844:410,461...424,809 		JBrowse link
G Prl prolactin ISO CTD Direct Evidence: marker/mechanism CTD PMID:240179 NCBI chrNW_004624756:4,585,542...4,593,285 JBrowse link
G Ptgs2 prostaglandin-endoperoxide synthase 2 ISO mRNA, protein:increased expression:neostriatum RGD PMID:15306248 PMID:16781689 PMID:21376018 RGD:5508224 RGD:5688225 RGD:5688269 NCBI chrNW_004624814:6,897,818...6,904,890
Ensembl chrNW_004624814:6,897,857...6,903,728 		JBrowse link
G Ptrhd1 peptidyl-tRNA hydrolase domain containing 1 ISO ClinVar Annotator: match by term: Parkinsonian disorder ClinVar PMID:27134041 PMID:27753167 PMID:29143421 NCBI chrNW_004624738:7,144,475...7,148,287
Ensembl chrNW_004624738:7,140,799...7,148,979 		JBrowse link
G Rela RELA proto-oncogene, NF-kB subunit ISO RGD PMID:18534259 RGD:2302392 NCBI chrNW_004624767:20,732,813...20,742,016
Ensembl chrNW_004624767:20,732,938...20,741,272 		JBrowse link
G Ret ret proto-oncogene ISO mRNA:altered expression:brain RGD PMID:12210101 RGD:6218972 NCBI chrNW_004624922:382,462...413,227
Ensembl chrNW_004624922:382,399...413,281 		JBrowse link
G Rgs4 regulator of G protein signaling 4 treatment ISO RGD PMID:25844489 RGD:13524517 NCBI chrNW_004624826:1,570,143...1,577,300
Ensembl chrNW_004624826:1,569,854...1,579,627 		JBrowse link
G Rgs9 regulator of G protein signaling 9 treatment ISO protein:decreased expression:striatum RGD PMID:18160641 PMID:20561938 PMID:21963945 RGD:13524532 RGD:13524862 RGD:13524864 NCBI chrNW_004624870:3,138,311...3,249,297
Ensembl chrNW_004624870:3,143,950...3,218,117 		JBrowse link
G Shh sonic hedgehog signaling molecule treatment ISO RGD PMID:25030123 RGD:12859032 NCBI chrNW_004624800:2,202,986...2,215,309
Ensembl chrNW_004624800:2,203,393...2,212,068 		JBrowse link
G Slc11a2 solute carrier family 11 member 2 ISO RGD PMID:19011085 PMID:20125122 RGD:5688713 RGD:5688715 NCBI chrNW_004624816:1,345,020...1,389,615
Ensembl chrNW_004624816:1,345,006...1,384,299 		JBrowse link
G Slc17a8 solute carrier family 17 member 8 ISO protein:increased expression:substantia nigra pars reticulata, neuron, perikaryon RGD PMID:17435391 RGD:9999153 NCBI chrNW_004624750:7,345,411...7,396,445
Ensembl chrNW_004624750:7,345,557...7,396,154 		JBrowse link
G Slc18a2 solute carrier family 18 member A2 ISO CTD Direct Evidence: therapeutic CTD PMID:16269145 NCBI chrNW_004624737:29,356,590...29,388,099
Ensembl chrNW_004624737:29,358,696...29,387,808 		JBrowse link
G Slc30a10 solute carrier family 30 member 10 ISO CTD Direct Evidence: marker/mechanism CTD PMID:26220508 NCBI chrNW_004624835:3,598,375...3,612,165
Ensembl chrNW_004624835:3,598,260...3,611,307 		JBrowse link
G Slc6a3 solute carrier family 6 member 3 ISO protein:decreased expression:striatum RGD PMID:15680936 RGD:1625663 NCBI chrNW_004624751:694,165...720,287
Ensembl chrNW_004624751:694,099...719,465 		JBrowse link
G Slc6a4 solute carrier family 6 member 4 ISO RGD PMID:20447560 RGD:4889474 NCBI chrNW_004624786:2,673,285...2,711,432
Ensembl chrNW_004624786:2,672,552...2,710,914 		JBrowse link
G Snca synuclein alpha ISO CTD Direct Evidence: marker/mechanism
mRNA:decreased expression:brain		 RGD
CTD		 PMID:15147505 PMID:15499605 PMID:20464527 PMID:22319455 PMID:23046578 More... RGD:6478799 RGD:6478802 NCBI chrNW_004624757:17,393,046...17,528,783
Ensembl chrNW_004624757:17,392,998...17,528,320 		JBrowse link
G Sncg synuclein gamma ISO RGD PMID:15147505 RGD:6478802 NCBI chrNW_004624841:192,396...196,568
Ensembl chrNW_004624841:192,398...196,064 		JBrowse link
G Src SRC proto-oncogene, non-receptor tyrosine kinase ISO RGD PMID:16529858 RGD:1581410 NCBI chrNW_004624842:2,212,561...2,260,514
Ensembl chrNW_004624842:2,211,020...2,230,132 		JBrowse link
G Tbc1d24 TBC1 domain family member 24 ISO ClinVar Annotator: match by term: Parkinsonian disorder ClinVar PMID:3402014 PMID:25401298 PMID:25741868 PMID:27281533 PMID:27541164 More... NCBI chrNW_004624824:245,717...251,603
Ensembl chrNW_004624824:243,939...254,249 		JBrowse link
G Tfam transcription factor A, mitochondrial ISO mRNA:increased expression:striatum RGD PMID:22040668 RGD:6484267 NCBI chrNW_004624791:5,183,276...5,198,986
Ensembl chrNW_004624791:5,179,195...5,198,611 		JBrowse link
G Tgm6 transglutaminase 6 ISO ClinVar Annotator: match by term: Parkinsonism ClinVar PMID:25741868 NCBI chrNW_004624741:3,654,288...3,672,382
Ensembl chrNW_004624741:3,646,131...3,672,382 		JBrowse link
G Th tyrosine hydroxylase treatment
susceptibility		 ISO protein:decreased expression:striatum
Segawa syndrome,autosomal recessive, OMIM:605407;DNA:missense mutation:exon:p.Q381L
CTD Direct Evidence: marker/mechanism		 RGD
CTD		 PMID:7814018 PMID:8817341 PMID:11246459 PMID:20561938 PMID:23831692 RGD:13524532 RGD:1601634 RGD:401700381 NCBI chrNW_004624767:15,003,073...15,010,207
Ensembl chrNW_004624767:15,003,092...15,010,154 		JBrowse link
G Tnf tumor necrosis factor treatment ISO RGD PMID:21831964 PMID:28338241 RGD:13503338 RGD:7247422 NCBI chrNW_004624754:24,623,059...24,625,647
Ensembl chrNW_004624754:24,623,425...24,625,531 		JBrowse link
G Tnfrsf1b TNF receptor superfamily member 1B treatment ISO RGD PMID:21831964 RGD:7247422 NCBI chrNW_004624818:894,470...922,806
Ensembl chrNW_004624818:896,150...922,710 		JBrowse link
G Ucn urocortin ISO RGD PMID:21362449 RGD:5508188 NCBI chrNW_004624738:9,393,004...9,393,966
Ensembl chrNW_004624738:9,393,329...9,393,706 		JBrowse link
G Vdac1 voltage dependent anion channel 1 ISO RGD PMID:24825319 RGD:13504672 NCBI chrNW_004624733:38,183,376...38,210,368
Ensembl chrNW_004624733:38,184,016...38,210,478 		JBrowse link
G Vhl von Hippel-Lindau tumor suppressor ISO RGD PMID:20302395 RGD:2325190 NCBI chrNW_004624731:5,350,912...5,359,286 JBrowse link
G Vip vasoactive intestinal peptide ISO RGD PMID:15808913 RGD:5685601 NCBI chrNW_004624785:5,466,429...5,487,763
Ensembl chrNW_004624785:5,468,563...5,488,143 		JBrowse link
amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Park7 Parkinsonism associated deglycase ISO ClinVar Annotator: match by term: Guam disease ClinVar PMID:25741868 NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Trpm7 transient receptor potential cation channel subfamily M member 7 susceptibility
no_association		 ISO ClinVar Annotator: match by term: Guam disease
DNA:mutation:cds: p.T1482I (human)		 OMIM
ClinVar
RGD		 PMID:19405049 PMID:25741868 PMID:28492532 RGD:5685008 NCBI chrNW_004624731:9,490,885...9,588,255
Ensembl chrNW_004624731:9,491,157...9,588,346 		JBrowse link
Autosomal Dominant Diffuse Lewy Body Disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gba1 glucosylceramidase beta 1 ISO ClinVar Annotator: match by term: Autosomal dominant diffuse Lewy body disease ClinVar PMID:1348297 PMID:1704891 PMID:1897529 PMID:1899336 PMID:1961718 More... NCBI chrNW_004624885:2,315,371...2,321,327
Ensembl chrNW_004624885:2,315,142...2,321,327 		JBrowse link
G Snca synuclein alpha ISO ClinVar Annotator: match by term: Autosomal dominant diffuse Lewy body disease ClinVar PMID:25393002 PMID:28492532 NCBI chrNW_004624757:17,393,046...17,528,783
Ensembl chrNW_004624757:17,392,998...17,528,320 		JBrowse link
G Sncb synuclein beta ISO ClinVar Annotator: match by term: Autosomal dominant diffuse Lewy body disease ClinVar PMID:15365127 PMID:21045828 PMID:25741868 PMID:26332674 PMID:31589614 More... NCBI chrNW_004624733:13,506,181...13,513,979
Ensembl chrNW_004624733:13,506,180...13,513,712 		JBrowse link
classic dopamine transporter deficiency syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Slc6a3 solute carrier family 6 member 3 ISO ClinVar Annotator: match by term: Classic dopamine transporter deficiency syndrome | ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile, 1 OMIM
ClinVar		 PMID:10889530 PMID:16103889 PMID:16171832 PMID:16199547 PMID:16212992 More... NCBI chrNW_004624751:694,165...720,287
Ensembl chrNW_004624751:694,099...719,465 		JBrowse link
dopamine transporter deficiency syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ahrr aryl-hydrocarbon receptor repressor ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:128,596...212,170
Ensembl chrNW_004624751:139,085...209,546 		JBrowse link
G Brd9 bromodomain containing 9 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:421,945...439,146
Ensembl chrNW_004624751:421,154...439,544 		JBrowse link
G Cep72 centrosomal protein 72 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:332,428...352,664 JBrowse link
G Clptm1l CLPTM1 like ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:652,857...669,400
Ensembl chrNW_004624751:652,767...669,587 		JBrowse link
G Exoc3 exocyst complex component 3 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:215,762...254,200
Ensembl chrNW_004624751:215,821...255,104 		JBrowse link
G Irx4 iroquois homeobox 4 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:913,127...916,583
Ensembl chrNW_004624751:913,691...916,842 		JBrowse link
G Lpcat1 lysophosphatidylcholine acyltransferase 1 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:732,364...764,421
Ensembl chrNW_004624751:730,472...764,430 		JBrowse link
G Mrpl36 mitochondrial ribosomal protein L36 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:871,163...872,596
Ensembl chrNW_004624751:871,158...872,498 		JBrowse link
G Ndufs6 NADH:ubiquinone oxidoreductase subunit S6 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:873,575...880,266
Ensembl chrNW_004624751:873,599...880,266 		JBrowse link
G Nkd2 NKD inhibitor of WNT signaling pathway 2 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:495,561...507,756 JBrowse link
G Pdcd6 programmed cell death 6 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:99,835...120,963
Ensembl chrNW_004624751:99,860...120,963 		JBrowse link
G Sdha succinate dehydrogenase complex flavoprotein subunit A ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:54,778...90,457
Ensembl chrNW_004624751:54,779...90,447 		JBrowse link
G Slc12a7 solute carrier family 12 member 7 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:508,902...544,319
Ensembl chrNW_004624751:506,040...544,365 		JBrowse link
G Slc6a18 solute carrier family 6 member 18 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:608,834...617,995
Ensembl chrNW_004624751:608,766...619,213 		JBrowse link
G Slc6a19 solute carrier family 6 member 19 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:591,846...606,362
Ensembl chrNW_004624751:591,754...607,693 		JBrowse link
G Slc6a3 solute carrier family 6 member 3 ISO ClinVar Annotator: match by term: DOPAMINE TRANSPORTER DEFICIENCY SYNDROME | ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:9536098 PMID:10889530 PMID:16103889 PMID:16171832 PMID:16199547 More... NCBI chrNW_004624751:694,165...720,287
Ensembl chrNW_004624751:694,099...719,465 		JBrowse link
G Slc9a3 solute carrier family 9 member A3 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:254,373...290,218
Ensembl chrNW_004624751:256,305...291,178 		JBrowse link
G Tert telomerase reverse transcriptase ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:624,569...647,198 JBrowse link
G Tppp tubulin polymerization promoting protein ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:355,887...375,564
Ensembl chrNW_004624751:355,890...375,561 		JBrowse link
G Trip13 thyroid hormone receptor interactor 13 ISO ClinVar Annotator: match by term: Parkinsonism-dystonia, infantile ClinVar PMID:21112253 PMID:28492532 NCBI chrNW_004624751:439,195...459,033
Ensembl chrNW_004624751:439,119...459,080 		JBrowse link
early-onset Parkinson's disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Lrrk2 leucine rich repeat kinase 2 ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:15680455 PMID:15680456 PMID:15680457 PMID:15726496 PMID:15732108 More... NCBI chrNW_004624778:106,594...279,325
Ensembl chrNW_004624778:108,761...279,230 		JBrowse link
G Pacrg parkin coregulated ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:12707451 PMID:12730996 PMID:15606901 PMID:16643317 PMID:19636047 More... NCBI chrNW_004624855:99,475...430,105 JBrowse link
G Park7 Parkinsonism associated deglycase ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:25741868 NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Prkn parkin RBR E3 ubiquitin protein ligase ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:10072423 PMID:10824074 PMID:11179010 PMID:11558785 PMID:11889248 More... NCBI chrNW_004624855:430,148...1,992,121
Ensembl chrNW_004624855:430,260...1,989,747 		JBrowse link
G Vps13c vacuolar protein sorting 13 homolog C ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:25741868 PMID:26942284 NCBI chrNW_004624781:10,259,971...10,414,421
Ensembl chrNW_004624781:10,259,976...10,413,278 		JBrowse link
infantile parkinsonism-dystonia 2 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Slc18a2 solute carrier family 18 member A2 ISO ClinVar Annotator: match by term: Brain dopamine-serotonin vesicular transport disease OMIM
ClinVar		 PMID:25741868 PMID:26497564 PMID:26539891 PMID:28492532 PMID:28716265 More... NCBI chrNW_004624737:29,356,590...29,388,099
Ensembl chrNW_004624737:29,358,696...29,387,808 		JBrowse link
INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND EARLY-ONSET DOPA-RESPONSIVE DYSTONIA-PARKINSONISM term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Nr4a2 nuclear receptor subfamily 4 group A member 2 ISO ClinVar Annotator: match by term: Intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism OMIM
ClinVar		 PMID:25741868 PMID:29758562 PMID:29770430 PMID:31428396 PMID:31922365 More... NCBI chrNW_004624732:9,572,160...9,589,624
Ensembl chrNW_004624732:9,581,779...9,589,942 		JBrowse link
juvenile-onset Parkinson's disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Pacrg parkin coregulated ISO ClinVar Annotator: match by term: Juvenile-onset Parkinson disease ClinVar NCBI chrNW_004624855:99,475...430,105 JBrowse link
G Park7 Parkinsonism associated deglycase ISO ClinVar Annotator: match by term: Juvenile-onset Parkinson disease ClinVar NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Prkn parkin RBR E3 ubiquitin protein ligase ISO ClinVar Annotator: match by term: Juvenile-onset Parkinson disease ClinVar PMID:25741868 NCBI chrNW_004624855:430,148...1,992,121
Ensembl chrNW_004624855:430,260...1,989,747 		JBrowse link
G Tnfrsf9 TNF receptor superfamily member 9 ISO ClinVar Annotator: match by term: Juvenile-onset Parkinson disease ClinVar NCBI chrNW_004624818:3,924,883...3,934,343
Ensembl chrNW_004624818:3,925,626...3,934,046 		JBrowse link
Kufor-Rakeb syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp13a2 ATPase cation transporting 13A2 ISO ClinVar Annotator: match by term: Kufor-Rakeb syndrome OMIM
ClinVar		 PMID:495089 PMID:9536098 PMID:12169656 PMID:16199547 PMID:16964263 More... NCBI chrNW_004624764:2,614,541...2,631,972
Ensembl chrNW_004624764:2,614,827...2,631,793 		JBrowse link
late onset Parkinson's disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atxn2 ataxin 2 susceptibility ISO OMIM NCBI chrNW_004624747:20,603,319...20,728,346
Ensembl chrNW_004624747:20,590,906...20,727,962 		JBrowse link
G Atxn3 ataxin 3 ISO OMIM NCBI chrNW_004624734:8,685,994...8,726,329 JBrowse link
G Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624800:1,174,703...1,234,661
Ensembl chrNW_004624800:1,175,679...1,234,951 		JBrowse link
G Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar PMID:24218364 PMID:25118025 PMID:27270108 NCBI chrNW_004624730:8,497,781...8,649,058
Ensembl chrNW_004624730:8,517,998...8,648,318 		JBrowse link
G Eif4g1 eukaryotic translation initiation factor 4 gamma 1 ISO ClinVar Annotator: match by term: Parkinson disease 18, autosomal dominant, susceptibility to OMIM
ClinVar		 PMID:21907011 PMID:23408866 PMID:25368108 PMID:25741868 PMID:28492532 NCBI chrNW_004624730:72,251,840...72,271,724 JBrowse link
G Fgf20 fibroblast growth factor 20 ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar PMID:18252210 PMID:19133659 PMID:25741868 NCBI chrNW_004624769:22,325,936...22,334,608
Ensembl chrNW_004624769:22,310,396...22,334,182 		JBrowse link
G Gba1 glucosylceramidase beta 1 ISO ClinVar Annotator: match by term: Hereditary late onset Parkinson disease | ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar
OMIM		 PMID:1333717 PMID:1348297 PMID:1415223 PMID:1487244 PMID:1558964 More... NCBI chrNW_004624885:2,315,371...2,321,327
Ensembl chrNW_004624885:2,315,142...2,321,327 		JBrowse link
G LOC101706353 HLA class II histocompatibility antigen, DR alpha chain ISO DNA:SNP:intron: (rs3129882) (human) RGD PMID:21791235 RGD:5490156 NCBI chrNW_004624754:24,079,459...24,086,342
Ensembl chrNW_004624754:24,079,366...24,084,512 		JBrowse link
G Lrrk2 leucine rich repeat kinase 2 ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar PMID:15680455 PMID:15680456 PMID:15680457 PMID:15726496 PMID:15732108 More... NCBI chrNW_004624778:106,594...279,325
Ensembl chrNW_004624778:108,761...279,230 		JBrowse link
G Mapt microtubule associated protein tau ISO ClinVar Annotator: match by term: Hereditary late onset Parkinson disease | ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar
OMIM		 PMID:2273997 PMID:8673924 PMID:9382467 PMID:9629852 PMID:9641683 More... NCBI chrNW_004624849:2,320,887...2,421,099 JBrowse link
G Nr4a2 nuclear receptor subfamily 4 group A member 2 ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar PMID:12496759 PMID:15079038 PMID:15184637 PMID:19429166 PMID:23066323 More... NCBI chrNW_004624732:9,572,160...9,589,624
Ensembl chrNW_004624732:9,581,779...9,589,942 		JBrowse link
G Park7 Parkinsonism associated deglycase ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Pink1 PTEN induced kinase 1 ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar NCBI chrNW_004624764:5,656,207...5,671,260
Ensembl chrNW_004624764:5,656,229...5,671,260 		JBrowse link
G Podxl podocalyxin like ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar PMID:26864383 PMID:28492532 NCBI chrNW_004624783:4,840,072...4,888,709
Ensembl chrNW_004624783:4,840,164...4,888,705 		JBrowse link
G Psap prosaposin ISO ClinVar Annotator: match by term: PARKINSON DISEASE 24, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | ClinVar Annotator: match by term: Parkinson disease 24, autosomal dominant, susceptibility to | ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar
OMIM		 PMID:2019586 PMID:9536098 PMID:17576681 PMID:19955343 PMID:25741868 More... NCBI chrNW_004624754:5,725,697...5,753,575
Ensembl chrNW_004624754:5,726,681...5,753,575 		JBrowse link
G Sncaip synuclein alpha interacting protein ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar PMID:12761037 PMID:18366718 PMID:25741868 PMID:28492532 NCBI chrNW_004624774:19,702,884...19,853,952
Ensembl chrNW_004624774:19,702,565...19,827,374 		JBrowse link
G Tbp TATA-box binding protein ISO OMIM NCBI chrNW_004624850:6,359,382...6,375,391
Ensembl chrNW_004624850:6,359,418...6,375,391 		JBrowse link
G Vps35 VPS35 retromer complex component ISO ClinVar Annotator: match by term: Parkinson disease, late-onset ClinVar NCBI chrNW_004624914:160,483...188,534
Ensembl chrNW_004624914:160,483...188,490 		JBrowse link
Lewy body dementia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ager advanced glycosylation end-product specific receptor ISO CTD Direct Evidence: marker/mechanism CTD PMID:16141792 NCBI chrNW_004624754:24,138,086...24,140,900 JBrowse link
G Aif1 allograft inflammatory factor 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624754:24,590,071...24,591,913
Ensembl chrNW_004624754:24,590,071...24,591,904 		JBrowse link
G Anxa5 annexin A5 ISO protein:increased expression: plasma RGD PMID:23576984 RGD:10053729 NCBI chrNW_004624777:1,921,354...1,969,772
Ensembl chrNW_004624777:1,919,602...1,970,059 		JBrowse link
G Apoe apolipoprotein E ISO protein:increased expression:neuron: RGD PMID:21907175 RGD:7771591 NCBI chrNW_004624907:1,752,322...1,755,308 JBrowse link
G Becn1 beclin 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19628769 NCBI chrNW_004624795:1,386,154...1,406,314
Ensembl chrNW_004624795:1,385,756...1,405,714 		JBrowse link
G Chrna4 cholinergic receptor nicotinic alpha 4 subunit ISO RGD PMID:15465084 RGD:1358509 NCBI chrNW_004624741:29,024,668...29,039,684
Ensembl chrNW_004624741:29,026,908...29,044,464 		JBrowse link
G Chrna7 cholinergic receptor nicotinic alpha 7 subunit ISO RGD PMID:15465084 RGD:1358509 NCBI chrNW_004624768:908,907...1,024,953
Ensembl chrNW_004624768:909,099...1,024,902 		JBrowse link
G Edn1 endothelin 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624756:13,842,482...13,849,003
Ensembl chrNW_004624756:13,842,164...13,849,029 		JBrowse link
G Elk1 ETS transcription factor ELK1 ISO RGD PMID:20126313 RGD:7488914 NCBI chrNW_004624978:194,985...208,105
Ensembl chrNW_004624978:194,992...208,103 		JBrowse link
G Eno2 enolase 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:30236862 NCBI chrNW_004624860:3,553,936...3,561,343
Ensembl chrNW_004624860:3,553,947...3,564,294 		JBrowse link
G Gba1 glucosylceramidase beta 1 ISO ClinVar Annotator: match by term: Diffuse Lewy body disease | ClinVar Annotator: match by term: Lewy body dementia ClinVar
OMIM		 PMID:1301953 PMID:1333717 PMID:1348297 PMID:1415223 PMID:1487244 More... NCBI chrNW_004624885:2,315,371...2,321,327
Ensembl chrNW_004624885:2,315,142...2,321,327 		JBrowse link
G Gfap glial fibrillary acidic protein ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624795:395,298...400,781
Ensembl chrNW_004624795:394,436...401,231 		JBrowse link
G Gpr37 G protein-coupled receptor 37 ISO RGD PMID:14991825 RGD:13504666 NCBI chrNW_004624783:11,291,601...11,319,467
Ensembl chrNW_004624783:11,291,497...11,320,952 		JBrowse link
G Igf1r insulin like growth factor 1 receptor ISO mRNA:altered expression:brain:
CTD Direct Evidence: marker/mechanism		 RGD
CTD		 PMID:19276553 RGD:5129515 NCBI chrNW_004624768:5,396,027...5,688,435
Ensembl chrNW_004624768:5,396,156...5,681,809 		JBrowse link
G Igf2 insulin like growth factor 2 ISO CTD Direct Evidence: marker/mechanism
mRNA:decreased expression:frontal cortex		 CTD
RGD		 PMID:19276553 RGD:5129515 NCBI chrNW_004624767:14,969,977...14,997,577
Ensembl chrNW_004624767:14,969,866...14,979,026 		JBrowse link
G Igf2r insulin like growth factor 2 receptor ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624855:2,752,676...2,887,327
Ensembl chrNW_004624855:2,753,994...2,887,151 		JBrowse link
G Ins insulin ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624767:14,999,088...15,000,035
Ensembl chrNW_004624767:14,999,088...15,000,035 		JBrowse link
G Insr insulin receptor ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624828:345,135...485,856
Ensembl chrNW_004624828:345,135...486,184 		JBrowse link
G Klk6 kallikrein related peptidase 6 ISO RGD PMID:12928483 RGD:1358597 NCBI chrNW_004624832:3,785,727...3,793,078
Ensembl chrNW_004624832:3,785,644...3,793,074 		JBrowse link
G LOC101724812 C-C chemokine receptor type 1 ISO RGD PMID:14595653 RGD:5688166 NCBI chrNW_004624730:74,822,848...74,828,614
Ensembl chrNW_004624730:74,826,659...74,827,726 		JBrowse link
G Mag myelin associated glycoprotein ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624794:8,237,005...8,251,933
Ensembl chrNW_004624794:8,236,223...8,258,361 		JBrowse link
G Map2 microtubule associated protein 2 ISO CTD Direct Evidence: marker/mechanism RGD
CTD		 PMID:20024519 PMID:30236862 RGD:6483091 NCBI chrNW_004624765:6,476,544...6,758,959
Ensembl chrNW_004624765:6,476,346...6,546,116 		JBrowse link
G Mmrn1 multimerin 1 ISO ClinVar Annotator: match by term: Lewy body dementia ClinVar PMID:14593171 PMID:14755720 PMID:15451224 PMID:15451225 PMID:16358335 More... NCBI chrNW_004624757:17,652,112...17,721,030
Ensembl chrNW_004624757:17,628,421...17,724,327 		JBrowse link
G Nefl neurofilament light chain ISO protein:increased expression:CSF (human) RGD PMID:29368621 PMID:29391125 RGD:127284889 RGD:127285384 NCBI chrNW_004624758:20,063,109...20,068,459
Ensembl chrNW_004624758:20,062,685...20,068,609 		JBrowse link
G Ngf nerve growth factor ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624772:11,009,765...11,070,050
Ensembl chrNW_004624772:11,010,845...11,070,017 		JBrowse link
G Ngfr nerve growth factor receptor ISO protein:decreased expression:brain RGD PMID:8347330 RGD:10413896 NCBI chrNW_004624795:5,623,686...5,639,545
Ensembl chrNW_004624795:5,623,700...5,639,655 		JBrowse link
G Nos2 nitric oxide synthase 2 ISO RGD PMID:10674474 RGD:1358529 NCBI chrNW_004624786:491,944...530,427
Ensembl chrNW_004624786:489,311...528,271 		JBrowse link
G Ntrk1 neurotrophic receptor tyrosine kinase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624885:1,989,027...2,005,474
Ensembl chrNW_004624885:1,989,138...2,005,577 		JBrowse link
G Ntrk2 neurotrophic receptor tyrosine kinase 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624809:8,274,736...8,622,287
Ensembl chrNW_004624809:8,276,951...8,616,765 		JBrowse link
G Pcna proliferating cell nuclear antigen ISO protein:increased expression:Hippocampal sub ventricular zone,Subgranular layer: RGD PMID:20665591 RGD:10448971 NCBI chrNW_004624741:6,143,584...6,148,055
Ensembl chrNW_004624741:6,143,332...6,148,898 		JBrowse link
G Ppargc1a PPARG coactivator 1 alpha ISO CTD Direct Evidence: marker/mechanism CTD PMID:30236862 NCBI chrNW_004624755:7,826,219...8,460,746
Ensembl chrNW_004624755:8,375,596...8,465,297 		JBrowse link
G Prkn parkin RBR E3 ubiquitin protein ligase ISO RGD PMID:17467279 RGD:10412737 NCBI chrNW_004624855:430,148...1,992,121
Ensembl chrNW_004624855:430,260...1,989,747 		JBrowse link
G Septin4 septin 4 ISO RGD PMID:12695511 RGD:13504670 NCBI chrNW_004624871:330,225...402,327 JBrowse link
G Snca synuclein alpha ISO ClinVar Annotator: match by term: Lewy Body Disease | ClinVar Annotator: match by term: Lewy body dementia OMIM
ClinVar		 PMID:9197268 PMID:9499430 PMID:9506559 PMID:9536098 PMID:9827625 More... NCBI chrNW_004624757:17,393,046...17,528,783
Ensembl chrNW_004624757:17,392,998...17,528,320 		JBrowse link
G Sncb synuclein beta ISO ClinVar Annotator: match by term: Diffuse Lewy body disease | ClinVar Annotator: match by term: Lewy body dementia OMIM
ClinVar		 PMID:15365127 PMID:21045828 PMID:25741868 PMID:26332674 PMID:31589614 More... NCBI chrNW_004624733:13,506,181...13,513,979
Ensembl chrNW_004624733:13,506,180...13,513,712 		JBrowse link
G Sncg synuclein gamma ISO protein:increased expression:cerebrospinal fluid
protein:increased expression:hippocampus		 RGD PMID:10557341 PMID:18577885 PMID:20697047 RGD:6478704 RGD:6478792 RGD:6480095 NCBI chrNW_004624841:192,396...196,568
Ensembl chrNW_004624841:192,398...196,064 		JBrowse link
G Sod2 superoxide dismutase 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:16141792 NCBI chrNW_004624855:3,260,800...3,271,864
Ensembl chrNW_004624855:3,260,809...3,271,367 		JBrowse link
G Tardbp TAR DNA binding protein ISO RGD PMID:20669025 RGD:5687180 NCBI chrNW_004624818:1,759,496...1,789,806
Ensembl chrNW_004624818:1,759,497...1,789,813 		JBrowse link
G Th tyrosine hydroxylase ISO CTD Direct Evidence: marker/mechanism CTD PMID:30236862 NCBI chrNW_004624767:15,003,073...15,010,207
Ensembl chrNW_004624767:15,003,092...15,010,154 		JBrowse link
G Vcp valosin containing protein ISO ClinVar Annotator: match by term: Lewy body dementia ClinVar PMID:28492532 NCBI chrNW_004624915:253,240...270,440
Ensembl chrNW_004624915:253,240...270,501 		JBrowse link
MPTP Poisoning term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aqp9 aquaporin 9 ISO CTD Direct Evidence: marker/mechanism CTD PMID:29566083 NCBI chrNW_004624781:13,650,612...13,691,175
Ensembl chrNW_004624781:13,648,065...13,691,260 		JBrowse link
G Il17a interleukin 17A ISO CTD Direct Evidence: marker/mechanism CTD PMID:31351185 NCBI chrNW_004624855:3,911,349...3,914,214
Ensembl chrNW_004624855:3,911,349...3,913,136 		JBrowse link
G Ins insulin ISO CTD Direct Evidence: therapeutic CTD PMID:26364587 NCBI chrNW_004624767:14,999,088...15,000,035
Ensembl chrNW_004624767:14,999,088...15,000,035 		JBrowse link
NEURODEVELOPMENTAL DISORDER WITH EARLY-ONSET PARKINSONISM AND BEHAVIORAL ABNORMALITIES term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ptrhd1 peptidyl-tRNA hydrolase domain containing 1 ISO ClinVar Annotator: match by term: Neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities OMIM
ClinVar		 PMID:25741868 PMID:27134041 PMID:27753167 PMID:29143421 PMID:30398675 More... NCBI chrNW_004624738:7,144,475...7,148,287
Ensembl chrNW_004624738:7,140,799...7,148,979 		JBrowse link
Parkinson's disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Abl1 ABL proto-oncogene 1, non-receptor tyrosine kinase ISO protein:increased expression:brain:
protein:increased phosphorylation:striatum:		 RGD PMID:20823226 PMID:24412932 RGD:8693409 RGD:8693592 NCBI chrNW_004624760:4,878,811...5,032,719
Ensembl chrNW_004624760:4,878,556...5,031,491 		JBrowse link
G Ache acetylcholinesterase (Cartwright blood group) ISO RGD PMID:19474411 RGD:5509846 NCBI chrNW_004624740:16,275,108...16,280,639
Ensembl chrNW_004624740:16,275,117...16,281,793 		JBrowse link
G Adarb2 adenosine deaminase RNA specific B2 (inactive) ISO CTD Direct Evidence: marker/mechanism CTD PMID:25475535 NCBI chrNW_004624775:9,089,839...9,646,985
Ensembl chrNW_004624775:9,090,545...9,643,355 		JBrowse link
G Adcy5 adenylate cyclase 5 ISO OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251 MouseDO NCBI chrNW_004624912:1,632,469...1,767,885
Ensembl chrNW_004624912:1,632,107...1,768,462 		JBrowse link
G Afdn afadin, adherens junction formation factor ISO protein:decreased expression: caudate-putamen, substantia nigra RGD PMID:23393160 RGD:13838733 NCBI chrNW_004624785:11,549,805...11,698,029
Ensembl chrNW_004624785:11,551,687...11,697,921 		JBrowse link
G Agtr1 angiotensin II receptor type 1 ISO protein:decreased expression:caudate nucleus,putamen,substantia nigra: RGD PMID:8666063 RGD:10047397 NCBI chrNW_004624730:25,964,848...26,006,468
Ensembl chrNW_004624730:25,964,811...26,006,463 		JBrowse link
G Aif1 allograft inflammatory factor 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624754:24,590,071...24,591,913
Ensembl chrNW_004624754:24,590,071...24,591,904 		JBrowse link
G Akt1 AKT serine/threonine kinase 1 no_association ISO protein:altered expression:brain
DNA:SNPs, haplotype:introns:multiple (human)
DNA:SNPs:introns:multiple (human)		 RGD PMID:18395980 PMID:19800394 PMID:21741444 RGD:5509064 RGD:5509074 RGD:5509076 NCBI chrNW_004624734:507,880...525,295
Ensembl chrNW_004624734:509,368...525,295 		JBrowse link
G Aldh2 aldehyde dehydrogenase 2 family member ISO CTD Direct Evidence: marker/mechanism CTD PMID:24491970 NCBI chrNW_004624747:20,407,190...20,438,605
Ensembl chrNW_004624747:20,403,717...20,438,690 		JBrowse link
G Anxa5 annexin A5 ISO protein:decreased expression:cerebrospinal fluid: RGD PMID:10584677 RGD:10053728 NCBI chrNW_004624777:1,921,354...1,969,772
Ensembl chrNW_004624777:1,919,602...1,970,059 		JBrowse link
G Apaf1 apoptotic peptidase activating factor 1 ISO RGD PMID:24835407 RGD:13503333 NCBI chrNW_004624750:8,835,521...8,940,957
Ensembl chrNW_004624750:8,837,037...8,938,009 		JBrowse link
G Apoa1 apolipoprotein A1 ISO protein: altered expression: cerebrospinal fluid: 2 different isoforms RGD PMID:20085559 RGD:5508216 NCBI chrNW_004624784:12,249,283...12,251,215
Ensembl chrNW_004624784:12,249,283...12,251,136 		JBrowse link
G Apoe apolipoprotein E ISO protein:increased expression:neuron: RGD PMID:21907175 RGD:7771591 NCBI chrNW_004624907:1,752,322...1,755,308 JBrowse link
G Arpc3 actin related protein 2/3 complex subunit 3 treatment ISO RGD PMID:20713051 RGD:11049454 NCBI chrNW_004624747:21,438,602...21,451,154
Ensembl chrNW_004624747:21,438,612...21,454,753 		JBrowse link
G Atg7 autophagy related 7 ISO OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251 MouseDO NCBI chrNW_004624943:231,978...480,933
Ensembl chrNW_004624943:232,618...481,290 		JBrowse link
G Atm ATM serine/threonine kinase ISO protein:increased serine phosphorylation:cingulate gyrus RGD PMID:20502937 RGD:10053605 NCBI chrNW_004624784:2,933,172...3,080,131
Ensembl chrNW_004624784:2,937,499...3,078,216 		JBrowse link
G Atp13a2 ATPase cation transporting 13A2 ISO CTD Direct Evidence: marker/mechanism CTD
RGD		 PMID:23628791 PMID:25149416 PMID:26223426 RGD:10450518 NCBI chrNW_004624764:2,614,541...2,631,972
Ensembl chrNW_004624764:2,614,827...2,631,793 		JBrowse link
G Axin2 axin 2 ameliorates ISO RGD PMID:31078578 RGD:151356747 NCBI chrNW_004624870:2,803,743...2,832,489
Ensembl chrNW_004624870:2,800,873...2,832,626 		JBrowse link
G B2m beta-2-microglobulin ISO protein:increased expression:corpus striatum RGD PMID:7605592 RGD:6482706 NCBI chrNW_004624804:11,514,728...11,521,625 JBrowse link
G Bag5 BAG cochaperone 5 ISO CTD Direct Evidence: marker/mechanism CTD PMID:28348719 NCBI chrNW_004624734:1,315,052...1,320,627 JBrowse link
G Bdnf brain derived neurotrophic factor no_association ISO DNA:polymorphisms: :196G>A (p.V66M), 270C>T (human)
protein:decreased expression:substantia nigra pars compacta:
CTD Direct Evidence: marker/mechanism		 RGD
CTD		 PMID:10208589 PMID:16565926 PMID:19276553 RGD:10059346 RGD:8657025 NCBI chrNW_004624766:17,281,882...17,330,601
Ensembl chrNW_004624766:17,279,630...17,330,490 		JBrowse link
G Bglap bone gamma-carboxyglutamate protein ISO protein:decreased expression:serum RGD PMID:16114020 RGD:7207224 NCBI chrNW_004624885:1,526,625...1,528,235
Ensembl chrNW_004624885:1,527,538...1,528,109 		JBrowse link
G Bst1 bone marrow stromal cell antigen 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19915576 NCBI chrNW_004624755:16,123,705...16,161,814
Ensembl chrNW_004624755:16,134,640...16,150,816 		JBrowse link
G Casp9 caspase 9 ISO protein:increased activity:blood, leukocyte RGD PMID:16505307 RGD:13503345 NCBI chrNW_004624764:1,769,270...1,789,399
Ensembl chrNW_004624764:1,773,455...1,789,423 		JBrowse link
G Cast calpastatin ISO protein:decreased expression:substantia nigra, dopaminergic neuron
DNA:SNP:intron: (rs1559085) (human)		 RGD PMID:10722997 PMID:20127884 RGD:5509800 RGD:5683320 NCBI chrNW_004624743:15,265,930...15,405,904
Ensembl chrNW_004624743:15,346,837...15,403,150 		JBrowse link
G Cck cholecystokinin no_association ISO RGD PMID:10668930 RGD:1626086 NCBI chrNW_004624730:77,310,080...77,314,258
Ensembl chrNW_004624730:77,309,633...77,314,384 		JBrowse link
G Ccn2 cellular communication network factor 2 ISO protein:increased expression:substantia nigra (rat) RGD PMID:19463894 RGD:2314505 NCBI chrNW_004624753:6,022,033...6,024,866
Ensembl chrNW_004624753:6,023,069...6,024,833 		JBrowse link
G Chrnb3 cholinergic receptor nicotinic beta 3 subunit susceptibility ISO DNA:SNP:promoter: c.-57A>G(human) RGD PMID:24731518 RGD:405849280 NCBI chrNW_004624780:481,836...510,192
Ensembl chrNW_004624780:487,006...510,056 		JBrowse link
G Cntnap2 contactin associated protein 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25475535 NCBI chrNW_004624800:7,182,588...9,280,407
Ensembl chrNW_004624800:7,181,020...9,279,678 		JBrowse link
G Col19a1 collagen type XIX alpha 1 chain ISO CTD Direct Evidence: marker/mechanism CTD PMID:25475535 NCBI chrNW_004624819:9,668,052...10,023,511
Ensembl chrNW_004624819:9,673,233...9,996,628 		JBrowse link
G Cp ceruloplasmin ISO CTD Direct Evidence: marker/mechanism CTD PMID:19159062 PMID:25758665 NCBI chrNW_004624730:26,458,554...26,510,796
Ensembl chrNW_004624730:26,462,550...26,511,078 		JBrowse link
G Creb1 cAMP responsive element binding protein 1 ISO protein:decreased phosphorylation:striatum RGD PMID:25583483 RGD:401960857 NCBI chrNW_004624765:8,374,160...8,436,969 JBrowse link
G Crh corticotropin releasing hormone ISO protein:decreased expression:cerebral cortex (human) RGD PMID:3502064 RGD:5508835 NCBI chrNW_004624744:25,194,458...25,196,658
Ensembl chrNW_004624744:25,194,495...25,196,488 		JBrowse link
G Cripto cripto, EGF-CFC family member treatment ISO RGD PMID:20641036 RGD:11561895 NCBI chrNW_004624730:74,547,226...74,550,526 JBrowse link
G Crp C-reactive protein ISO RGD PMID:22426659 RGD:6482307 NCBI chrNW_004624794:1,531,555...1,533,804
Ensembl chrNW_004624794:1,531,571...1,533,804 		JBrowse link
G Dbh dopamine beta-hydroxylase susceptibility ISO protein:increased expression:frontal cortex (human)
DNA:snp:5' utr:g.-1021C>T (human)		 RGD PMID:14991826 PMID:19276553 RGD:1358583 RGD:5129515 NCBI chrNW_004624760:2,016,066...2,030,240
Ensembl chrNW_004624760:2,015,474...2,029,939 		JBrowse link
G Dbn1 drebrin 1 treatment ISO levodopainduced; protein:increased expression:striatum: RGD PMID:23241013 RGD:10398811 NCBI chrNW_004624733:12,616,537...12,631,967
Ensembl chrNW_004624733:12,616,423...12,632,133 		JBrowse link
G Ddc dopa decarboxylase ISO human gene in a rat model
CTD Direct Evidence: therapeutic
protein:altered expression:arcuate nucleus ((rat)		 RGD
CTD		 PMID:2969953 PMID:9853519 PMID:11445284 PMID:12703659 PMID:15935614 RGD:4139893 RGD:5129121 RGD:5129231 NCBI chrNW_004624740:3,674,727...3,732,058
Ensembl chrNW_004624740:3,674,609...3,732,676 		JBrowse link
G Ddit4 DNA damage inducible transcript 4 ISO CTD Direct Evidence: therapeutic CTD PMID:17005863 NCBI chrNW_004624754:6,091,914...6,094,035
Ensembl chrNW_004624754:6,091,809...6,094,525 		JBrowse link
G Ddost dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit ISO ClinVar Annotator: match by term: Parkinson Disease, Recessive ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624764:5,671,724...5,681,729
Ensembl chrNW_004624764:5,671,724...5,681,835 		JBrowse link
G Ddr2 discoidin domain receptor tyrosine kinase 2 treatment ISO RGD PMID:28863860 RGD:150519888 NCBI chrNW_004624826:1,225,217...1,255,889
Ensembl chrNW_004624826:1,173,621...1,249,692 		JBrowse link
G Dlg1 discs large MAGUK scaffold protein 1 ISO protein:altered localization, decreased expression:striatum:redistribution from synapse to vesicles RGD PMID:15703272 RGD:2306834 NCBI chrNW_004624730:62,001,547...62,223,098
Ensembl chrNW_004624730:62,002,280...62,223,319 		JBrowse link
G Dlg4 discs large MAGUK scaffold protein 4 ISO protein:altered localization, decreased expression:striatum:redistribution from synapse to vesicles RGD PMID:15703272 RGD:2306834 NCBI chrNW_004624786:9,811,201...9,835,660
Ensembl chrNW_004624786:9,811,780...9,837,100 		JBrowse link
G Dnajb6 DnaJ heat shock protein family (Hsp40) member B6 ISO ClinVar Annotator: match by term: Susceptibility to Parkinson's Disease ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624800:1,174,703...1,234,661
Ensembl chrNW_004624800:1,175,679...1,234,951 		JBrowse link
G Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 ISO RGD PMID:25701813 RGD:10450845 NCBI chrNW_004624730:8,497,781...8,649,058
Ensembl chrNW_004624730:8,517,998...8,648,318 		JBrowse link
G Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 ISO RGD PMID:25639775 RGD:10450521 NCBI chrNW_004624742:29,397,811...29,525,886
Ensembl chrNW_004624742:29,398,544...29,485,165 		JBrowse link
G Dnm1l dynamin 1 like ISO CTD Direct Evidence: marker/mechanism CTD PMID:28215578 NCBI chrNW_004624778:3,391,690...3,475,548 JBrowse link
G Draxin dorsal inhibitory axon guidance protein ISO CTD Direct Evidence: marker/mechanism CTD PMID:25475535 NCBI chrNW_004624818:1,253,968...1,274,418
Ensembl chrNW_004624818:1,256,169...1,263,904 		JBrowse link
G Drd1 dopamine receptor D1 treatment ISO CTD Direct Evidence: therapeutic
protein:decreased expression:striatum (rat)		 RGD
CTD		 PMID:8558425 PMID:16365282 PMID:23041629 RGD:7248455 RGD:7248595 NCBI chrNW_004624733:14,517,540...14,522,173
Ensembl chrNW_004624733:14,518,146...14,520,905 		JBrowse link
G Drd2 dopamine receptor D2 ISO protein:increased expression:striatum (rat)
OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251
CTD Direct Evidence: therapeutic		 RGD
MouseDO
CTD		 PMID:8558425 PMID:18289173 RGD:2311585 NCBI chrNW_004624784:8,828,589...8,906,617
Ensembl chrNW_004624784:8,827,006...8,865,529 		JBrowse link
G Drd3 dopamine receptor D3 severity ISO protein:increased expression:blood, lymphocyte
mRNA:decreased expression:blood, lymphocyte		 RGD PMID:8618685 PMID:10495037 RGD:5686418 RGD:5686419 NCBI chrNW_004624731:34,318,733...34,369,111
Ensembl chrNW_004624731:34,319,130...34,363,184 		JBrowse link
G Drd5 dopamine receptor D5 ISO protein:increased expression:blood, lymphocyte RGD PMID:10495037 RGD:5686418 NCBI chrNW_004624755:21,358,586...21,361,410 JBrowse link
G Edn1 endothelin 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624756:13,842,482...13,849,003
Ensembl chrNW_004624756:13,842,164...13,849,029 		JBrowse link
G Egfr epidermal growth factor receptor ISO protein:decreased expression:forebrain RGD PMID:15857400 RGD:2289955 NCBI chrNW_004624740:584,133...713,205
Ensembl chrNW_004624740:589,606...713,271 		JBrowse link
G Eif2ak2 eukaryotic translation initiation factor 2 alpha kinase 2 ISO RGD PMID:15567511 RGD:10395348 NCBI chrNW_004624738:18,716,623...18,764,243
Ensembl chrNW_004624738:18,717,092...18,758,457 		JBrowse link
G En1 engrailed homeobox 1 ISO DNA:SNP:enhancer: (rs1438852) (human) RGD
MouseDO		 PMID:19345444 RGD:5687197 NCBI chrNW_004624732:26,333,642...26,338,450
Ensembl chrNW_004624732:26,333,653...26,337,904 		JBrowse link
G Eno2 enolase 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:30236862 NCBI chrNW_004624860:3,553,936...3,561,343
Ensembl chrNW_004624860:3,553,947...3,564,294 		JBrowse link
G Ephx1 epoxide hydrolase 1 no_association ISO DNA:missense mutation:exon:p.Y113H (human)
DNA:missense mutations:exons:p.Y113H (499T>C), p.H139R (578A>G) (human)		 RGD PMID:10720475 PMID:11692079 RGD:5490167 RGD:5688390 NCBI chrNW_004624835:6,161,930...6,181,016
Ensembl chrNW_004624835:6,162,111...6,168,714 		JBrowse link
G Ephx2 epoxide hydrolase 2 no_association ISO DNA:missense mutation, insertion:exons:p.R287Q (898G>A), p.S402_R403insR (1246_1247insTCG) (human) RGD PMID:11692079 RGD:5688390 NCBI chrNW_004624758:22,216,462...22,252,467
Ensembl chrNW_004624758:22,221,314...22,254,813 		JBrowse link
G Erbb2 erb-b2 receptor tyrosine kinase 2 ISO protein:decreased expression:forebrain RGD PMID:15857400 RGD:2289955 NCBI chrNW_004624795:3,373,313...3,391,509
Ensembl chrNW_004624795:3,373,000...3,391,602 		JBrowse link
G Esr2 estrogen receptor 2 onset ISO DNA:polymorphism: :1730A>G(human) RGD PMID:15219649 RGD:5508776 NCBI chrNW_004624734:36,742,913...36,862,993
Ensembl chrNW_004624734:36,759,104...36,825,295 		JBrowse link
G Fas Fas cell surface death receptor ISO protein:decreased expression:neurones of the substantia nigra pars: RGD PMID:11054182 RGD:12903948 NCBI chrNW_004624791:15,290,022...15,315,848
Ensembl chrNW_004624791:15,289,348...15,315,848 		JBrowse link
G Faslg Fas ligand ISO protein:decreased expression:neurones of the substantia nigra pars:
protein:increased expression:substantia nigra pars compacta, striatum (rat)		 RGD PMID:11054182 PMID:17959308 RGD:12903948 RGD:2290172 NCBI chrNW_004624771:9,031,978...9,038,760
Ensembl chrNW_004624771:9,032,016...9,038,825 		JBrowse link
G Fbp1 fructose-bisphosphatase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:18353766 NCBI chrNW_004624753:16,019,546...16,048,096
Ensembl chrNW_004624753:16,016,022...16,048,104 		JBrowse link
G Fbxo7 F-box protein 7 ISO ClinVar Annotator: match by term: Parkinson Disease, Recessive ClinVar PMID:25741868 NCBI chrNW_004624750:1,977,666...1,997,408
Ensembl chrNW_004624750:1,977,761...1,997,231 		JBrowse link
G Fcer2 Fc fragment of IgE receptor II ISO CTD Direct Evidence: marker/mechanism CTD PMID:25475535 NCBI chrNW_004624828:747,800...754,185
Ensembl chrNW_004624828:748,671...754,185 		JBrowse link
G Fez1 fasciculation and elongation protein zeta 1 ISO RGD PMID:23888906 RGD:13208826 NCBI chrNW_004624927:1,470,218...1,512,780
Ensembl chrNW_004624927:1,469,025...1,512,790 		JBrowse link
G Fgb fibrinogen beta chain ISO CTD Direct Evidence: marker/mechanism CTD PMID:23233872 NCBI chrNW_004624858:5,866,104...5,874,173
Ensembl chrNW_004624858:5,864,784...5,874,869 		JBrowse link
G Gak cyclin G associated kinase ISO CTD Direct Evidence: marker/mechanism CTD PMID:20711177 NCBI chrNW_004624755:26,208,207...26,250,937
Ensembl chrNW_004624755:26,208,334...26,250,533 		JBrowse link
G Gba1 glucosylceramidase beta 1 no_association
onset		 ISO DNA:missense mutations:cds:p.K-26R, p.K186R, p.N370S (human)
ClinVar Annotator: match by term: Susceptibility to Parkinson's Disease
ClinVar Annotator: match by term: Parkinson Disease, Recessive | ClinVar Annotator: match by term: Susceptibility to Parkinson's Disease
DNA:missense mutation:cds:p.N370S (human)		 RGD
ClinVar		 PMID:1348297 PMID:1704891 PMID:1897529 PMID:1899336 PMID:1961718 More... RGD:5508427 RGD:5508429 NCBI chrNW_004624885:2,315,371...2,321,327
Ensembl chrNW_004624885:2,315,142...2,321,327 		JBrowse link
G Gdf5 growth differentiation factor 5 treatment ISO mRNA:increased expression:striatum: RGD PMID:22436046 PMID:24373993 RGD:12738227 RGD:12738228 NCBI chrNW_004624842:3,958,814...3,963,713
Ensembl chrNW_004624842:3,959,617...3,963,020 		JBrowse link
G Gdnf glial cell derived neurotrophic factor ISO mRNA:increased expression:putamen
CTD Direct Evidence: therapeutic		 RGD
CTD		 PMID:11031079 PMID:16324109 PMID:16644101 RGD:6218968 NCBI chrNW_004624759:17,263,570...17,290,046
Ensembl chrNW_004624759:17,263,969...17,287,723 		JBrowse link
G Gfap glial fibrillary acidic protein ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624795:395,298...400,781
Ensembl chrNW_004624795:394,436...401,231 		JBrowse link
G Gjc2 gap junction protein gamma 2 treatment ISO RGD PMID:21561882 RGD:13208520 NCBI chrNW_004624937:898,876...905,247 JBrowse link
G Gpr37 G protein-coupled receptor 37 ISO RGD PMID:14991825 RGD:13504666 NCBI chrNW_004624783:11,291,601...11,319,467
Ensembl chrNW_004624783:11,291,497...11,320,952 		JBrowse link
G Grk2 G protein-coupled receptor kinase 2 ISO Protein: decreased expression: brain RGD PMID:17996024 RGD:5685370 NCBI chrNW_004624767:19,212,218...19,231,218
Ensembl chrNW_004624767:19,210,965...19,231,082 		JBrowse link
G Grk3 G protein-coupled receptor kinase 3 ISO protein:decreased expression:caudate putamen (rat) RGD PMID:17996024 RGD:5685370 NCBI chrNW_004624747:1,567,540...1,758,251
Ensembl chrNW_004624747:1,576,681...1,758,201 		JBrowse link
G Grk5 G protein-coupled receptor kinase 5 no_association ISO protein: decreased expression: brain
DNA: snps: :rs871196, rs2420616, rs7069375, rs4752293		 RGD PMID:17125886 PMID:17996024 PMID:21184589 RGD:5685370 RGD:5688382 RGD:5688384 NCBI chrNW_004624737:27,379,114...27,600,132
Ensembl chrNW_004624737:27,375,149...27,600,210 		JBrowse link
G Grk6 G protein-coupled receptor kinase 6 ISO protein: decreased expression: brain
human gene in rat model		 RGD PMID:17996024 PMID:22090514 RGD:5684916 RGD:5685370 NCBI chrNW_004624733:12,633,565...12,661,284 JBrowse link
G Grn granulin precursor no_association ISO DNA:SNP:3' utr:*78C>T (rs5848) (human)
protein:decreased expression:serum		 RGD PMID:19473366 PMID:23398167 RGD:10401642 RGD:10401644 NCBI chrNW_004624795:704,066...708,721
Ensembl chrNW_004624795:704,252...707,165 		JBrowse link
G Gsk3b glycogen synthase kinase 3 beta treatment ISO RGD PMID:23094836 RGD:10045553 NCBI chrNW_004624731:28,178,647...28,368,784
Ensembl chrNW_004624731:28,178,628...28,366,420 		JBrowse link
G Gsta4 glutathione S-transferase alpha 4 ISO CTD Direct Evidence: marker/mechanism CTD PMID:16510128 NCBI chrNW_004624850:201,119...217,302
Ensembl chrNW_004624850:201,592...216,680 		JBrowse link
G Gsto1 glutathione S-transferase omega 1 onset
susceptibility		 ISO DNA:polymorphism:exon:p. A140D (rs4925) (human) RGD PMID:14570706 PMID:17194543 RGD:1358651 RGD:5490299 NCBI chrNW_004624831:3,342,539...3,351,766
Ensembl chrNW_004624831:3,342,584...3,352,467 		JBrowse link
G Hcn3 hyperpolarization activated cyclic nucleotide gated potassium channel 3 ISO mRNA:increased expression:neuron: RGD PMID:19320057 RGD:9693679 NCBI chrNW_004624885:2,271,991...2,281,575
Ensembl chrNW_004624885:2,272,935...2,281,588 		JBrowse link
G Hfe homeostatic iron regulator ISO CTD Direct Evidence: marker/mechanism CTD PMID:16824219 NCBI chrNW_004624756:821,738...831,482
Ensembl chrNW_004624756:823,947...831,376 		JBrowse link
G Hgf hepatocyte growth factor ISO CTD Direct Evidence: therapeutic CTD PMID:16791285 NCBI chrNW_004624739:30,233,589...30,307,508
Ensembl chrNW_004624739:30,236,146...30,307,356 		JBrowse link
G Hmgcr 3-hydroxy-3-methylglutaryl-CoA reductase ISO RGD PMID:18184918 RGD:5508459 NCBI chrNW_004624951:681,559...711,476
Ensembl chrNW_004624951:682,178...711,474 		JBrowse link
G Hmox1 heme oxygenase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:21318773 NCBI chrNW_004624750:341,699...346,005
Ensembl chrNW_004624750:342,146...345,887 		JBrowse link
G Hnmt histamine N-methyltransferase no_association ISO RGD PMID:17985251 PMID:19773194 RGD:5509775 RGD:5509778 NCBI chrNW_004624732:37,621,014...37,689,873
Ensembl chrNW_004624732:37,620,925...37,691,708 		JBrowse link
G Hsf1 heat shock transcription factor 1 treatment ISO protein:decreased expression:midbrain (rat) RGD PMID:24296154 PMID:24852355 RGD:10402545 RGD:10402753 NCBI chrNW_004624735:12,536,818...12,562,643
Ensembl chrNW_004624735:12,537,128...12,562,644 		JBrowse link
G Hspa4 heat shock protein family A (Hsp70) member 4 ISO protein:decreased expression:striatum (rat) RGD PMID:22186119 RGD:5686884 NCBI chrNW_004624733:39,022,511...39,068,153
Ensembl chrNW_004624733:39,021,738...39,068,132 		JBrowse link
G Hspa8 heat shock protein family A (Hsp70) member 8 ISO protein: increased expression: brain
protein: decreased expression		 RGD PMID:17241115 PMID:18704197 PMID:20697033 RGD:6218982 RGD:6480203 RGD:6480228 NCBI chrNW_004624880:2,070,410...2,075,069
Ensembl chrNW_004624880:2,070,523...2,079,421 		JBrowse link
G Hspa9 heat shock protein family A (Hsp70) member 9 disease_progression ISO protein:decreased expression:brain
CTD Direct Evidence: marker/mechanism
DNA:mutations:multiple:
DNA:mutation:cds:A>T476(human)		 RGD
CTD		 PMID:16565515 PMID:18219256 PMID:19657588 PMID:20817635 RGD:6784528 RGD:6784529 RGD:6784530 RGD:6784531 NCBI chrNW_004624743:31,324,085...31,345,681
Ensembl chrNW_004624743:31,324,085...31,345,695 		JBrowse link
G Hspd1 heat shock protein family D (Hsp60) member 1 ISO RGD PMID:23943523 RGD:10402846 NCBI chrNW_004624889:2,736,727...2,746,333 JBrowse link
G Htr1a 5-hydroxytryptamine receptor 1A ISO RGD PMID:20508280 RGD:5683633 NCBI chrNW_004624815:5,817,196...5,821,197
Ensembl chrNW_004624815:5,816,601...5,820,864 		JBrowse link
G Htra2 HtrA serine peptidase 2 no_association ISO DNA:missense mutation:cds:p.S276C (mouse)
DNA:missense mutation:cds:p.P143A (human)
DNA:missense mutation:cds:p.R404W (human)
DNA:missense mutation, transversion:cds, intron:p.G26E, g.IVS5+29T>A (human)
DNA:missense mutations:cds:p.A141S, p.G399S (human)		 RGD PMID:14534547 PMID:15509788 PMID:15961413 PMID:18364387 PMID:18401856 More... RGD:5688367 RGD:5688381 RGD:5688392 RGD:5688393 RGD:5688394 RGD:5688395 RGD:5688714 NCBI chrNW_004624749:28,980,375...28,983,719
Ensembl chrNW_004624749:28,980,362...28,983,869 		JBrowse link
G Htt huntingtin ISO RGD PMID:26192120 RGD:13452383 NCBI chrNW_004624755:24,602,955...24,729,584
Ensembl chrNW_004624755:24,603,490...24,729,333 		JBrowse link
G Igf1r insulin like growth factor 1 receptor ISO CTD Direct Evidence: marker/mechanism
mRNA:altered expression:brain:
protein: altered activity		 CTD
RGD		 PMID:19276553 PMID:19703168 RGD:5129515 RGD:5686429 NCBI chrNW_004624768:5,396,027...5,688,435
Ensembl chrNW_004624768:5,396,156...5,681,809 		JBrowse link
G Igf2 insulin like growth factor 2 ISO mRNA:decreased expression:frontal cortex
CTD Direct Evidence: marker/mechanism		 RGD
CTD		 PMID:19276553 RGD:5129515 NCBI chrNW_004624767:14,969,977...14,997,577
Ensembl chrNW_004624767:14,969,866...14,979,026 		JBrowse link
G Igf2r insulin like growth factor 2 receptor ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624855:2,752,676...2,887,327
Ensembl chrNW_004624855:2,753,994...2,887,151 		JBrowse link
G Il1b interleukin 1 beta ISO RGD PMID:12070246 PMID:23159314 RGD:1358742 RGD:7175549 NCBI chrNW_004624749:12,852,128...12,858,478
Ensembl chrNW_004624749:12,852,021...12,858,760 		JBrowse link
G Il6 interleukin 6 ISO CTD Direct Evidence: marker/mechanism CTD PMID:21318773 NCBI chrNW_004624739:7,957,709...7,963,414
Ensembl chrNW_004624739:7,957,674...7,962,318 		JBrowse link
G Ins insulin ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624767:14,999,088...15,000,035
Ensembl chrNW_004624767:14,999,088...15,000,035 		JBrowse link
G Insr insulin receptor ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624828:345,135...485,856
Ensembl chrNW_004624828:345,135...486,184 		JBrowse link
G Kcnj4 potassium inwardly rectifying channel subfamily J member 4 ISO CTD Direct Evidence: therapeutic CTD PMID:18619942 NCBI chrNW_004624752:9,633,799...9,659,532
Ensembl chrNW_004624752:9,638,704...9,659,523 		JBrowse link
G Kcnn2 potassium calcium-activated channel subfamily N member 2 ISO OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251 MouseDO NCBI chrNW_004624733:7,429,681...7,931,192
Ensembl chrNW_004624733:7,429,681...7,578,596 		JBrowse link
G Klk6 kallikrein related peptidase 6 ISO RGD PMID:12928483 RGD:1358597 NCBI chrNW_004624832:3,785,727...3,793,078
Ensembl chrNW_004624832:3,785,644...3,793,074 		JBrowse link
G L1cam L1 cell adhesion molecule ISO RGD PMID:19995872 RGD:6483033 NCBI chrNW_004624946:512,413...533,669
Ensembl chrNW_004624946:513,297...525,009 		JBrowse link
G Lep leptin treatment ISO rat protein in a mouse model RGD PMID:17895242 RGD:10053631 NCBI chrNW_004624783:7,708,820...7,721,610
Ensembl chrNW_004624783:7,708,588...7,721,727 		JBrowse link
G LOC101706353 HLA class II histocompatibility antigen, DR alpha chain onset ISO DNA:SNP:intron: (rs3129882) (human)
CTD Direct Evidence: marker/mechanism		 RGD
CTD		 PMID:20711177 RGD:5490158 NCBI chrNW_004624754:24,079,459...24,086,342
Ensembl chrNW_004624754:24,079,366...24,084,512 		JBrowse link
G LOC101707509 cytochrome P450 1A1 susceptibility
no_association		 ISO DNA:missense mutation:cds:p.I462V (human)
DNA:polymorphisms (human)		 RGD PMID:8872868 PMID:11484167 PMID:11793160 RGD:5147678 RGD:5147679 RGD:5147681 NCBI chrNW_004627988:7...1,323 JBrowse link
G LOC101722366 cytochrome P450 2E1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:16510128 NCBI chrNW_004624737:12,335,733...12,345,278
Ensembl chrNW_004624737:12,335,681...12,345,514 		JBrowse link
G LOC101726271 protoheme IX farnesyltransferase, mitochondrial ISO OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251 MouseDO NCBI chrNW_004624877:2,161,819...2,282,336
Ensembl chrNW_004624877:2,161,885...2,282,615 		JBrowse link
G Lrrk2 leucine rich repeat kinase 2 no_association
susceptibility		 ISO DNA:missense mutation:cds:p.G2019S (human)
ClinVar Annotator: match by term: Parkinson Disease, Dominant | ClinVar Annotator: match by term: Parkinson disease
DNA:missense mutation:cds:p.R1398H (human)		 RGD
ClinVar		 PMID:15680455 PMID:15680456 PMID:15680457 PMID:15726496 PMID:15732108 More... RGD:5508406 RGD:5508409 NCBI chrNW_004624778:106,594...279,325
Ensembl chrNW_004624778:108,761...279,230 		JBrowse link
G Mag myelin associated glycoprotein ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624794:8,237,005...8,251,933
Ensembl chrNW_004624794:8,236,223...8,258,361 		JBrowse link
G Maoa monoamine oxidase A ISO CTD Direct Evidence: marker/mechanism CTD PMID:17449559 NCBI chrNW_004624762:11,743,833...11,820,529
Ensembl chrNW_004624762:11,743,712...11,822,377 		JBrowse link
G Maob monoamine oxidase B ISO CTD Direct Evidence: marker/mechanism
protein:increased activity:striatum (rat)		 CTD
RGD		 PMID:9129714 PMID:17417741 PMID:21318773 RGD:1358484 RGD:2316771 NCBI chrNW_004624762:11,584,925...11,720,273
Ensembl chrNW_004624762:11,584,825...11,720,506 		JBrowse link
G Map2 microtubule associated protein 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:30236862 NCBI chrNW_004624765:6,476,544...6,758,959
Ensembl chrNW_004624765:6,476,346...6,546,116 		JBrowse link
G Map3k5 mitogen-activated protein kinase kinase kinase 5 ISO CTD Direct Evidence: marker/mechanism CTD PMID:21815648 NCBI chrNW_004624886:970,415...1,189,595
Ensembl chrNW_004624886:969,623...1,190,709 		JBrowse link
G Mapk1 mitogen-activated protein kinase 1 ISO protein:decreased phosphorylation:striatum RGD PMID:25583483 RGD:401960857 NCBI chrNW_004624747:1,296,062...1,389,674
Ensembl chrNW_004624747:1,296,221...1,389,757 		JBrowse link
G Mapk3 mitogen-activated protein kinase 3 ISO protein:decreased phosphorylation:striatum RGD PMID:25583483 RGD:401960857 NCBI chrNW_004624782:13,150,824...13,158,327
Ensembl chrNW_004624782:13,152,039...13,159,113 		JBrowse link
G Mapt microtubule associated protein tau susceptibility ISO DNA:SNP:intron: (rs8070723) (human)
ClinVar Annotator: match by term: Susceptibility to Parkinson's Disease		 RGD
ClinVar		 PMID:2273997 PMID:8673924 PMID:9382467 PMID:9629852 PMID:9641683 More... RGD:8158107 NCBI chrNW_004624849:2,320,887...2,421,099 JBrowse link
G Minar2 membrane integral NOTCH2 associated receptor 2 ISO MouseDO NCBI chrNW_004624774:11,607,603...11,623,582
Ensembl chrNW_004624774:11,607,504...11,623,544 		JBrowse link
G Mthfr methylenetetrahydrofolate reductase ISO CTD Direct Evidence: marker/mechanism CTD PMID:30726997 NCBI chrNW_004624818:1,184,736...1,202,708
Ensembl chrNW_004624818:1,187,869...1,199,168 		JBrowse link
G Mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase susceptibility ISO DNA:polymorphism: :1049A>G (human) RGD PMID:21070756 RGD:5508183 NCBI chrNW_004624751:5,445,274...5,469,386
Ensembl chrNW_004624751:5,445,241...5,469,657 		JBrowse link
G Nanog Nanog homeobox treatment ISO mouse gene in a rat model;mRNA, protein:increased expression:embryonic stem cell RGD PMID:24954161 RGD:9681444 NCBI chrNW_004624860:5,026,203...5,037,219 JBrowse link
G Ncapg2 non-SMC condensin II complex subunit G2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25475535 NCBI chrNW_004624800:432,307...494,361
Ensembl chrNW_004624800:432,258...498,718 		JBrowse link
G Ndufa13 NADH:ubiquinone oxidoreductase subunit A13 ISO RGD PMID:26605748 RGD:13504667 NCBI chrNW_004624908:2,311,801...2,319,604
Ensembl chrNW_004624908:2,312,452...2,319,604 		JBrowse link
G Ndufb8 NADH:ubiquinone oxidoreductase subunit B8 ISO RGD PMID:26605748 RGD:13504667 NCBI chrNW_004624831:195,552...200,458
Ensembl chrNW_004624831:191,625...200,860 		JBrowse link
G Ndufs1 NADH:ubiquinone oxidoreductase core subunit S1 onset ISO protein:increased oxidation:brain, mitochondrion (mouse) RGD PMID:21196577 RGD:6484690 NCBI chrNW_004624765:9,962,254...9,993,790
Ensembl chrNW_004624765:9,962,447...9,993,790 		JBrowse link
G Ndufs4 NADH:ubiquinone oxidoreductase subunit S4 ISO RGD PMID:21383081 RGD:6484691 NCBI chrNW_004624759:5,630,522...5,733,928 JBrowse link
G Ndufv2 NADH:ubiquinone oxidoreductase core subunit V2 susceptibility ISO DNA:polymorphism: :p.A29V RGD PMID:9570948 RGD:2302386 NCBI chrNW_004624770:17,925,250...17,950,754 JBrowse link
G Nectin2 nectin cell adhesion molecule 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25475535 NCBI chrNW_004624907:1,713,786...1,739,158
Ensembl chrNW_004624907:1,713,443...1,740,627 		JBrowse link
G Nedd8 NEDD8 ubiquitin like modifier ISO RGD PMID:12533840 RGD:1549458 NCBI chrNW_004624820:8,319,763...8,329,748
Ensembl chrNW_004624820:8,319,832...8,329,748 		JBrowse link
G Nefl neurofilament light chain ISO protein:increased expression:CSF (human) RGD PMID:29391125 RGD:127285384 NCBI chrNW_004624758:20,063,109...20,068,459
Ensembl chrNW_004624758:20,062,685...20,068,609 		JBrowse link
G Ngf nerve growth factor ISO CTD Direct Evidence: marker/mechanism CTD PMID:19276553 NCBI chrNW_004624772:11,009,765...11,070,050
Ensembl chrNW_004624772:11,010,845...11,070,017 		JBrowse link
G Ngfr nerve growth factor receptor ISO protein:decreased expression:brain RGD PMID:8347330 RGD:10413896 NCBI chrNW_004624795:5,623,686...5,639,545
Ensembl chrNW_004624795:5,623,700...5,639,655 		JBrowse link
G Nos1 nitric oxide synthase 1 ISO CTD Direct Evidence: marker/mechanism
RNA, protein:increased expression:neutrophil		 CTD
RGD		 PMID:11020342 PMID:11809160 PMID:26383258 RGD:1358519 RGD:5132632 NCBI chrNW_004624747:15,940,614...16,118,051
Ensembl chrNW_004624747:16,003,969...16,113,165 		JBrowse link
G Nos2 nitric oxide synthase 2 ISO protein:increased expression:striatum (mouse) RGD PMID:21970803 RGD:5509573 NCBI chrNW_004624786:491,944...530,427
Ensembl chrNW_004624786:489,311...528,271 		JBrowse link
G Nox1 NADPH oxidase 1 ameliorates ISO RGD PMID:23077033 RGD:329961565 NCBI chrNW_004624902:1,741,921...1,754,932
Ensembl chrNW_004624902:1,736,704...1,755,504 		JBrowse link
G Nqo1 NAD(P)H quinone dehydrogenase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:17188257 NCBI chrNW_004624746:16,684,620...16,698,194
Ensembl chrNW_004624746:16,684,407...16,697,479 		JBrowse link
G Nqo2 N-ribosyldihydronicotinamide:quinone dehydrogenase 2 susceptibility ISO DNA:deletion:promoter: (human) RGD PMID:18314446 RGD:11073691 NCBI chrNW_004624756:21,857,048...21,869,657
Ensembl chrNW_004624756:21,857,721...21,867,727 		JBrowse link
G Nr4a1 nuclear receptor subfamily 4 group A member 1 treatment ISO compared to wild-type and untreated RGD PMID:29530712 RGD:40924655 NCBI chrNW_004624816:271,345...288,265
Ensembl chrNW_004624816:267,303...293,227 		JBrowse link
G Nr4a2 nuclear receptor subfamily 4 group A member 2 ISO ClinVar Annotator: match by term: Parkinson Disease, Dominant/Recessive | ClinVar Annotator: match by term: Parkinson's disease ClinVar PMID:23066323 PMID:28492532 NCBI chrNW_004624732:9,572,160...9,589,624
Ensembl chrNW_004624732:9,581,779...9,589,942 		JBrowse link
G Ntsr1 neurotensin receptor 1 ISO RGD PMID:7700529 RGD:9743906 NCBI chrNW_004624741:28,504,814...28,543,592
Ensembl chrNW_004624741:28,505,037...28,544,122 		JBrowse link
G Ogg1 8-oxoguanine DNA glycosylase ISO protein:increased expression:substantia nigra, neuron RGD PMID:15841414 RGD:8657142 NCBI chrNW_004624731:4,383,000...4,388,486
Ensembl chrNW_004624731:4,383,434...4,388,196 		JBrowse link
G Optn optineurin ISO protein:increased expression:substantia nigra (rat) RGD PMID:27473339 RGD:13432580 NCBI chrNW_004624805:5,683,095...5,717,558
Ensembl chrNW_004624805:5,683,021...5,721,336 		JBrowse link
G Park7 Parkinsonism associated deglycase onset ISO DNA:missense mutation, deletion: :L166P
ClinVar Annotator: match by term: Parkinson Disease, Recessive		 RGD
ClinVar		 PMID:12851414 PMID:12953260 PMID:20981092 PMID:25741868 PMID:26467025 More... RGD:1601073 NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Parp1 poly(ADP-ribose) polymerase 1 susceptibility
no_association		 ISO DNA:polymorphisms:promoter, exon:g.-410C>T, g.845_846dupAC (human)
DNA:snps:multiple (human)		 RGD PMID:17362997 PMID:21767974 RGD:5510021 RGD:5510024 NCBI chrNW_004624807:446,662...478,571
Ensembl chrNW_004624807:446,647...479,069 		JBrowse link
G Penk proenkephalin ISO mRNA:increased expression:striatum: RGD PMID:11501038 RGD:10003114 NCBI chrNW_004624886:3,595,485...3,613,117
Ensembl chrNW_004624886:3,595,450...3,613,593 		JBrowse link
G Phactr2 phosphatase and actin regulator 2 ISO DNA: snp: intron: rs11155313 RGD PMID:19429005 RGD:6483095 NCBI chrNW_004624753:10,456,910...10,742,311 JBrowse link
G Pink1 PTEN induced kinase 1 ISO ClinVar Annotator: match by term: Parkinson Disease, Recessive ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624764:5,656,207...5,671,260
Ensembl chrNW_004624764:5,656,229...5,671,260 		JBrowse link
G Pitx3 paired like homeodomain 3 ISO OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251 RGD
MouseDO		 PMID:18573342 RGD:11535079 NCBI chrNW_004624831:1,649,585...1,651,729
Ensembl chrNW_004624831:1,650,381...1,651,699 		JBrowse link
G Pla2g6 phospholipase A2 group VI no_association
onset		 ISO DNA:missense mutation:cds:p.P806R (c.2417C>G) (human)
DNA:missense muations, nonsense mutation: :p.F72L, p.Q452X, p.R635Q (human)		 RGD PMID:20938027 PMID:21368765 RGD:6482733 RGD:6482734 NCBI chrNW_004624752:9,792,778...9,841,817
Ensembl chrNW_004624752:9,792,807...9,843,457 		JBrowse link
G Polg DNA polymerase gamma, catalytic subunit onset ISO associated with Ophthalmoplegia, Chronic Progressive External;DNA:mutation:cds:p.K512M(human)
associated with Ophthalmoplegia, Chronic Progressive External;DNA:mutations: :
DNA:missense mutations:exons:p.R853W,p.G737R(human)		 RGD PMID:15351195 PMID:16634032 PMID:23865558 RGD:8694175 RGD:8694201 RGD:8694203 NCBI chrNW_004624768:16,493,123...16,509,747
Ensembl chrNW_004624768:16,491,555...16,509,900 		JBrowse link
G Ppargc1a PPARG coactivator 1 alpha onset ISO CTD Direct Evidence: marker/mechanism
DNA:SNPs:intron, 3' utr: (rs2970848, rs6821591) (human)		 CTD
MouseDO
RGD		 PMID:21376232 PMID:21595954 PMID:30236862 RGD:6484270 RGD:6484271 NCBI chrNW_004624755:7,826,219...8,460,746
Ensembl chrNW_004624755:8,375,596...8,465,297 		JBrowse link
G Ppp1r9b protein phosphatase 1 regulatory subunit 9B ISO protein:altered localization:striate nucleus (rat) RGD PMID:18372251 RGD:10043801 NCBI chrNW_004624795:6,124,273...6,137,776
Ensembl chrNW_004624795:6,124,159...6,137,955 		JBrowse link
G Ppp2ca protein phosphatase 2 catalytic subunit alpha ISO protein:decreased tyrosine phosphorylation:brain (human) RGD PMID:24395787 RGD:8693390 NCBI chrNW_004624733:38,012,694...38,033,745
Ensembl chrNW_004624733:38,012,392...38,036,914 		JBrowse link
G Prkn parkin RBR E3 ubiquitin protein ligase treatment ISO CTD Direct Evidence: marker/mechanism
DNA:mutations:multiple (human)
DNA:deletions:exons: (human)
protein:increased tyrosine-phosphorylation:substantia nigra, striatum, 		RGD
CTD		 PMID:9560156 PMID:12588799 PMID:12629236 PMID:15198987 PMID:15882845 More... RGD:10413859 RGD:10450518 RGD:10450521 RGD:13432207 RGD:13432563 RGD:13432567 RGD:737763 RGD:8693409 RGD:9693725 NCBI chrNW_004624855:430,148...1,992,121
Ensembl chrNW_004624855:430,260...1,989,747 		JBrowse link
G Ptgis prostaglandin I2 synthase treatment ISO human gene in a rat model RGD PMID:23691265 RGD:401959749 NCBI chrNW_004624790:5,850,647...5,885,754
Ensembl chrNW_004624790:5,850,810...5,886,014 		JBrowse link
G Ptn pleiotrophin treatment ISO RGD PMID:19615368 RGD:10044022 NCBI chrNW_004624765:17,523,086...17,625,264
Ensembl chrNW_004624765:17,522,916...17,548,184 		JBrowse link
G Rab32 RAB32, member RAS oncogene family ISO CTD Direct Evidence: marker/mechanism CTD PMID:38858457 NCBI chrNW_004624753:7,900,027...7,917,944
Ensembl chrNW_004624753:7,900,267...7,917,854 		JBrowse link
G Rpl14 ribosomal protein L14 ISO CTD Direct Evidence: marker/mechanism CTD PMID:18353766 NCBI chrNW_004624730:78,284,389...78,288,242
Ensembl chrNW_004624730:78,282,230...78,288,647 		JBrowse link
G Rpl23a ribosomal protein L23a ISO CTD Direct Evidence: marker/mechanism CTD PMID:18353766 NCBI chrNW_004624786:1,294,185...1,297,993 JBrowse link
G Rpl6 ribosomal protein L6 ISO CTD Direct Evidence: marker/mechanism CTD PMID:18353766 NCBI chrNW_004624747:19,821,875...19,826,605
Ensembl chrNW_004624747:19,822,791...19,827,045 		JBrowse link
G Rps8 ribosomal protein S8 ISO CTD Direct Evidence: marker/mechanism CTD PMID:18353766 NCBI chrNW_004624906:669,466...671,933
Ensembl chrNW_004624906:669,496...672,635 		JBrowse link
G Rrn3 RRN3 homolog, RNA polymerase I transcription factor ISO OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251 MouseDO NCBI chrNW_004624824:8,582,754...8,615,073
Ensembl chrNW_004624824:8,582,803...8,614,313 		JBrowse link
G S100b S100 calcium binding protein B ISO RGD PMID:21402140 PMID:21725169 RGD:5508763 RGD:5508766 NCBI chrNW_004624745:31,645,927...31,652,846
Ensembl chrNW_004624745:31,645,927...31,652,832 		JBrowse link
G Sdha succinate dehydrogenase complex flavoprotein subunit A ISO protein:decreased expression:substantia nigra, neuron RGD PMID:26605748 RGD:13504667 NCBI chrNW_004624751:54,778...90,457
Ensembl chrNW_004624751:54,779...90,447 		JBrowse link
G Septin14 septin 14 susceptibility ISO DNA:SNPs:promoter:rs10241628, rs11981883, rs77231105 (human) RGD PMID:27115672 RGD:13504669 NCBI chrNW_004624740:8,086,964...8,138,550
Ensembl chrNW_004624740:8,085,384...8,134,973 		JBrowse link
G Septin4 septin 4 ISO RGD PMID:12695511 RGD:13504670 NCBI chrNW_004624871:330,225...402,327 JBrowse link
G Serpinf1 serpin family F member 1 severity ISO protein:increased expression:serum, extracellular exosome (human) RGD PMID:31593110 RGD:27226691 NCBI chrNW_004624786:4,487,005...4,497,706
Ensembl chrNW_004624786:4,486,978...4,497,585 		JBrowse link
G Slc11a2 solute carrier family 11 member 2 ISO DNA:polymorphism:cds:1254T>C(human) RGD PMID:19011085 PMID:21777657 RGD:5688403 RGD:5688713 NCBI chrNW_004624816:1,345,020...1,389,615
Ensembl chrNW_004624816:1,345,006...1,384,299 		JBrowse link
G Slc18a2 solute carrier family 18 member A2 resistance ISO mRNA:decreased expression:substantia nigra (rat)
CTD Direct Evidence: marker/mechanism
DNA:snps:5' utr:g.-103C>A, g.-74C>T, g.-62G>A (human)
protein:decreased expression:putamen, caudate nucleus, striatum (human)		 RGD
CTD		 PMID:11463816 PMID:16112329 PMID:16269145 PMID:16339215 PMID:16421508 More... RGD:5129143 RGD:5131086 RGD:5131163 RGD:5131165 RGD:5131167 NCBI chrNW_004624737:29,356,590...29,388,099
Ensembl chrNW_004624737:29,358,696...29,387,808 		JBrowse link
G Slc30a10 solute carrier family 30 member 10 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25149416 NCBI chrNW_004624835:3,598,375...3,612,165
Ensembl chrNW_004624835:3,598,260...3,611,307 		JBrowse link
G Slc38a2 solute carrier family 38 member 2 ISO CTD Direct Evidence: therapeutic CTD PMID:35728354 NCBI chrNW_004624816:5,888,447...5,902,009
Ensembl chrNW_004624816:5,888,414...5,902,897 		JBrowse link
G Slc6a3 solute carrier family 6 member 3 ISO CTD Direct Evidence: marker/mechanism CTD PMID:9763484 PMID:16112329 PMID:16963468 PMID:19590691 NCBI chrNW_004624751:694,165...720,287
Ensembl chrNW_004624751:694,099...719,465 		JBrowse link
G Snca synuclein alpha ISO ClinVar Annotator: match by term: Parkinson Disease, Dominant | ClinVar Annotator: match by term: Parkinson Disease, Recessive ClinVar PMID:23427326 PMID:23457019 PMID:24047453 PMID:24752924 PMID:24936070 More... NCBI chrNW_004624757:17,393,046...17,528,783
Ensembl chrNW_004624757:17,392,998...17,528,320 		JBrowse link
G Sncaip synuclein alpha interacting protein ISO ClinVar Annotator: match by term: Parkinson Disease, Dominant/Recessive ClinVar PMID:12761037 PMID:18366718 PMID:21344240 PMID:24033266 PMID:25741868 More... NCBI chrNW_004624774:19,702,884...19,853,952
Ensembl chrNW_004624774:19,702,565...19,827,374 		JBrowse link
G Sncb synuclein beta onset ISO protein:increased expression:hippocampus
DNA:SNP: :rs1352303(human) 		RGD PMID:10557341 PMID:17556099 RGD:6478793 RGD:6480095 NCBI chrNW_004624733:13,506,181...13,513,979
Ensembl chrNW_004624733:13,506,180...13,513,712 		JBrowse link
G Sncg synuclein gamma ISO protein:increased expression:hippocampus RGD PMID:10557341 RGD:6480095 NCBI chrNW_004624841:192,396...196,568
Ensembl chrNW_004624841:192,398...196,064 		JBrowse link
G Sod1 superoxide dismutase 1 treatment ISO human gene in a rat model
CTD Direct Evidence: marker/mechanism|therapeutic		 RGD
CTD		 PMID:16353238 PMID:21318773 RGD:8655933 NCBI chrNW_004624745:20,032,003...20,037,958
Ensembl chrNW_004624745:20,032,011...20,037,958 		JBrowse link
G Sod2 superoxide dismutase 2 susceptibility ISO CTD Direct Evidence: marker/mechanism CTD
RGD		 PMID:11161607 PMID:17188257 PMID:18353766 PMID:25279756 RGD:13464352 NCBI chrNW_004624855:3,260,800...3,271,864
Ensembl chrNW_004624855:3,260,809...3,271,367 		JBrowse link
G Spr sepiapterin reductase ISO OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251 MouseDO NCBI chrNW_004624762:729,294...734,761
Ensembl chrNW_004624762:728,731...734,544 		JBrowse link
G Srrm2 serine/arginine repetitive matrix 2 ISO mRNA:splice variants:substantia nigra, amygdala, peripheral blood mononuclear cell (human) RGD PMID:20161708 RGD:11038728 NCBI chrNW_004624824:594,203...613,225
Ensembl chrNW_004624824:594,790...609,750 		JBrowse link
G Synj1 synaptojanin 1 ISO RGD PMID:25639775 RGD:10450521 NCBI chrNW_004624745:20,881,312...20,984,242
Ensembl chrNW_004624745:20,881,317...20,984,184 		JBrowse link
G Taldo1 transaldolase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:23233872 NCBI chrNW_004624766:21,758,821...21,766,052
Ensembl chrNW_004624766:21,758,821...21,766,027 		JBrowse link
G Tardbp TAR DNA binding protein ISO DNA:mutation:cds:p.A382T (human) RGD PMID:20551689 PMID:21667065 RGD:5687172 RGD:5687183 NCBI chrNW_004624818:1,759,496...1,789,806
Ensembl chrNW_004624818:1,759,497...1,789,813 		JBrowse link
G Tcn2 transcobalamin 2 ISO RGD PMID:20027219 RGD:11060125 NCBI chrNW_004624747:6,970,707...6,987,946
Ensembl chrNW_004624747:6,971,289...6,987,440 		JBrowse link
G Tfam transcription factor A, mitochondrial no_association
susceptibility		 ISO DNA:missense mutation, SNP:exon, intron:p.S12T, IVS4+113A>G (rs1937, rs2306604) (human)
OMIM:168600 | OMIM:300557 | OMIM:556500 | OMIM:602404 | OMIM:606852 | OMIM:607688 | OMIM:610297 | OMIM:613164 | OMIM:613643 | OMIM:614251
DNA:SNP:intron:IVS4+113A>G (rs2306604) (human)
DNA:missense mutation:exon:p.S12T (rs1937) (human)		 RGD
MouseDO		 PMID:17537576 PMID:18248889 PMID:19925850 RGD:14389730 RGD:6771184 RGD:6771185 NCBI chrNW_004624791:5,183,276...5,198,986
Ensembl chrNW_004624791:5,179,195...5,198,611 		JBrowse link
G Th tyrosine hydroxylase ISO CTD Direct Evidence: marker/mechanism
protein:decreased expression:striatum (human)
human gene in a rat model
protein:decreased expression:midbrain, neuron (rat)
protein:decreased expression:substantia nigra (mouse)		 CTD
RGD		 PMID:2573072 PMID:9853519 PMID:15857400 PMID:21323909 PMID:21376343 More... RGD:2289955 RGD:5128607 RGD:5128616 RGD:5129120 RGD:5129121 NCBI chrNW_004624767:15,003,073...15,010,207
Ensembl chrNW_004624767:15,003,092...15,010,154 		JBrowse link
G Tmem230 transmembrane protein 230 ISO CTD Direct Evidence: marker/mechanism CTD PMID:27270108 NCBI chrNW_004624741:6,133,251...6,142,366
Ensembl chrNW_004624741:6,135,252...6,142,469 		JBrowse link
G Tnf tumor necrosis factor ISO CTD Direct Evidence: marker/mechanism CTD PMID:21318773 NCBI chrNW_004624754:24,623,059...24,625,647
Ensembl chrNW_004624754:24,623,425...24,625,531 		JBrowse link
G Tnfrsf1b TNF receptor superfamily member 1B ISO mRNA:decreased expression:midbrain, dopaminergic neuron (mouse) RGD PMID:19780901 RGD:5130931 NCBI chrNW_004624818:894,470...922,806
Ensembl chrNW_004624818:896,150...922,710 		JBrowse link
G Tnk2 tyrosine kinase non receptor 2 ISO ClinVar Annotator: match by term: Parkinson disease ClinVar PMID:23686771 PMID:25741868 PMID:26595808 PMID:28492532 NCBI chrNW_004624730:61,237,653...61,272,499
Ensembl chrNW_004624730:61,236,983...61,273,166 		JBrowse link
G Tnr tenascin R ISO ClinVar Annotator: match by term: Parkinson disease ClinVar PMID:26122175 PMID:26595808 PMID:28492532 PMID:33278868 NCBI chrNW_004624771:6,291,202...6,725,737
Ensembl chrNW_004624771:6,519,091...6,717,947 		JBrowse link
G Trpm2 transient receptor potential cation channel subfamily M member 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:27957685 NCBI chrNW_004624745:29,757,267...29,809,607
Ensembl chrNW_004624745:29,757,106...29,806,795 		JBrowse link
G Twnk twinkle mtDNA helicase ISO MouseDO NCBI chrNW_004624831:592,475...597,388 JBrowse link
G Uchl1 ubiquitin C-terminal hydrolase L1 ISO ClinVar Annotator: match by term: Parkinson Disease, Dominant ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624761:25,786,028...25,797,641
Ensembl chrNW_004624761:25,784,257...25,797,549 		JBrowse link
G Vdac1 voltage dependent anion channel 1 ISO RGD PMID:24825319 RGD:13504672 NCBI chrNW_004624733:38,183,376...38,210,368
Ensembl chrNW_004624733:38,184,016...38,210,478 		JBrowse link
G Vdr vitamin D receptor onset ISO DNA:polymorphisms: :rs4334089, rs2853559(human) RGD PMID:21309754 RGD:13217419 NCBI chrNW_004624816:4,314,146...4,423,946
Ensembl chrNW_004624816:4,365,961...4,424,514 		JBrowse link
G Vip vasoactive intestinal peptide ISO RGD PMID:19476518 RGD:5685606 NCBI chrNW_004624785:5,466,429...5,487,763
Ensembl chrNW_004624785:5,468,563...5,488,143 		JBrowse link
G Vps13c vacuolar protein sorting 13 homolog C ISO ClinVar Annotator: match by term: Parkinson disease ClinVar PMID:25741868 PMID:26942284 NCBI chrNW_004624781:10,259,971...10,414,421
Ensembl chrNW_004624781:10,259,976...10,413,278 		JBrowse link
G Vps35 VPS35 retromer complex component ISO ClinVar Annotator: match by term: Parkinson Disease, Dominant | ClinVar Annotator: match by term: Parkinson disease ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624914:160,483...188,534
Ensembl chrNW_004624914:160,483...188,490 		JBrowse link
Parkinson's disease 1 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mmrn1 multimerin 1 ISO ClinVar Annotator: match by term: Autosomal dominant Parkinson disease 1 ClinVar PMID:14593171 PMID:14755720 PMID:15451224 PMID:15451225 PMID:16358335 More... NCBI chrNW_004624757:17,652,112...17,721,030
Ensembl chrNW_004624757:17,628,421...17,724,327 		JBrowse link
G Snca synuclein alpha ISO ClinVar Annotator: match by term: Autosomal dominant Parkinson disease 1 OMIM
ClinVar		 PMID:9197268 PMID:9462735 PMID:9499430 PMID:9506559 PMID:9827625 More... NCBI chrNW_004624757:17,393,046...17,528,783
Ensembl chrNW_004624757:17,392,998...17,528,320 		JBrowse link
Parkinson's Disease 11 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gigyf2 GRB10 interacting GYF protein 2 ISO ClinVar Annotator: match by term: GIGYF2-related condition | ClinVar Annotator: match by term: Parkinson disease 11, autosomal dominant, susceptibility to OMIM
ClinVar		 PMID:18358451 PMID:18923002 PMID:19133664 PMID:19250854 PMID:19279319 More... NCBI chrNW_004624843:5,391,725...5,538,980
Ensembl chrNW_004624843:5,420,352...5,537,217 		JBrowse link
Parkinson's Disease 13 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aup1 AUP1 lipid droplet regulating VLDL assembly factor ISO ClinVar Annotator: match by term: Parkinson disease 13, autosomal dominant, susceptibility to ClinVar PMID:18401856 PMID:18790661 PMID:25741868 NCBI chrNW_004624749:28,983,753...28,986,785
Ensembl chrNW_004624749:28,983,802...28,986,643 		JBrowse link
G Htra2 HtrA serine peptidase 2 ISO ClinVar Annotator: match by term: Parkinson disease 13, autosomal dominant, susceptibility to OMIM
ClinVar		 PMID:15961413 PMID:18364387 PMID:18401856 PMID:18790661 PMID:19118185 More... NCBI chrNW_004624749:28,980,375...28,983,719
Ensembl chrNW_004624749:28,980,362...28,983,869 		JBrowse link
G Loxl3 lysyl oxidase like 3 ISO ClinVar Annotator: match by term: Parkinson disease 13, autosomal dominant, susceptibility to ClinVar PMID:15961413 PMID:18364387 PMID:18790661 PMID:19118185 PMID:21163861 More... NCBI chrNW_004624749:28,959,682...28,980,428
Ensembl chrNW_004624749:28,960,593...28,980,428 		JBrowse link
Parkinson's disease 14 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Pla2g6 phospholipase A2 group VI ISO ClinVar Annotator: match by term: Autosomal recessive Parkinson disease 14 | ClinVar Annotator: match by term: DYSTONIA-PARKINSONISM, ADULT-ONSET OMIM
ClinVar		 PMID:2668131 PMID:16783378 PMID:18359254 PMID:18414213 PMID:18443314 More... NCBI chrNW_004624752:9,792,778...9,841,817
Ensembl chrNW_004624752:9,792,807...9,843,457 		JBrowse link
G Slc39a14 solute carrier family 39 member 14 ISO CTD Direct Evidence: marker/mechanism CTD PMID:36152728 NCBI chrNW_004624758:17,911,889...17,954,870
Ensembl chrNW_004624758:17,912,827...17,953,294 		JBrowse link
Parkinson's disease 15 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fbxo7 F-box protein 7 ISO ClinVar Annotator: match by term: Parkinsonian-pyramidal syndrome OMIM
ClinVar		 PMID:9536098 PMID:16199547 PMID:17576681 PMID:18513678 PMID:19038853 More... NCBI chrNW_004624750:1,977,666...1,997,408
Ensembl chrNW_004624750:1,977,761...1,997,231 		JBrowse link
Parkinson's disease 17 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mylk3 myosin light chain kinase 3 ISO ClinVar Annotator: match by term: Parkinson disease 17 ClinVar PMID:28492532 NCBI chrNW_004624914:200,914...251,699
Ensembl chrNW_004624914:198,803...239,427 		JBrowse link
G Vps35 VPS35 retromer complex component ISO ClinVar Annotator: match by term: Parkinson disease 17 OMIM
ClinVar		 PMID:9536098 PMID:17576681 PMID:18342564 PMID:21763482 PMID:21763483 More... NCBI chrNW_004624914:160,483...188,534
Ensembl chrNW_004624914:160,483...188,490 		JBrowse link
Parkinson's disease 19A term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dnajc6 DnaJ heat shock protein family (Hsp40) member C6 ISO ClinVar Annotator: match by term: Juvenile onset Parkinson disease 19A | ClinVar Annotator: match by term: PARK19 | ClinVar Annotator: match by term: Parkinson disease 19B, early-onset OMIM
ClinVar		 PMID:2256350 PMID:9536098 PMID:16199547 PMID:17576681 PMID:22563501 More... NCBI chrNW_004624742:29,397,811...29,525,886
Ensembl chrNW_004624742:29,398,544...29,485,165 		JBrowse link
Parkinson's disease 2 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gatad2b GATA zinc finger domain containing 2B ISO ClinVar Annotator: match by term: Parkinsonism, early onset, with diurnal fluctuation ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624885:3,297,191...3,375,908
Ensembl chrNW_004624885:3,362,823...3,375,179 		JBrowse link
G Lrrk2 leucine rich repeat kinase 2 ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:15680455 PMID:15680456 PMID:15680457 PMID:15726496 PMID:15732108 More... NCBI chrNW_004624778:106,594...279,325
Ensembl chrNW_004624778:108,761...279,230 		JBrowse link
G Pacrg parkin coregulated ISO ClinVar Annotator: match by term: Autosomal recessive juvenile Parkinson disease 2 | ClinVar Annotator: match by term: Parkinsonism, early onset, with diurnal fluctuation | ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:12116199 PMID:12707451 PMID:12730996 PMID:15606901 PMID:16328510 More... NCBI chrNW_004624855:99,475...430,105 JBrowse link
G Park7 Parkinsonism associated deglycase ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:25741868 NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Podxl podocalyxin like ISO ClinVar Annotator: match by term: Autosomal recessive juvenile Parkinson disease 2 ClinVar PMID:26864383 NCBI chrNW_004624783:4,840,072...4,888,709
Ensembl chrNW_004624783:4,840,164...4,888,705 		JBrowse link
G Prkn parkin RBR E3 ubiquitin protein ligase ISO ClinVar Annotator: match by term: Autosomal recessive juvenile Parkinson disease 2 | ClinVar Annotator: match by term: Parkinsonism, early onset, with diurnal fluctuation | ClinVar Annotator: match by term: Young-onset Parkinson disease OMIM
ClinVar		 PMID:7565830 PMID:9560156 PMID:9634531 PMID:9731209 PMID:9802278 More... NCBI chrNW_004624855:430,148...1,992,121
Ensembl chrNW_004624855:430,260...1,989,747 		JBrowse link
G Vps13c vacuolar protein sorting 13 homolog C ISO ClinVar Annotator: match by term: Young-onset Parkinson disease ClinVar PMID:25741868 PMID:26942284 NCBI chrNW_004624781:10,259,971...10,414,421
Ensembl chrNW_004624781:10,259,976...10,413,278 		JBrowse link
Parkinson's disease 20 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp5po ATP synthase peripheral stalk subunit OSCP ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,064,438...22,074,753
Ensembl chrNW_004624745:22,064,441...22,074,773 		JBrowse link
G Cfap298 cilia and flagella associated protein 298 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,862,313...20,877,188
Ensembl chrNW_004624745:20,862,538...20,876,646 		JBrowse link
G Clic6 chloride intracellular channel 6 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,807,618...22,861,521
Ensembl chrNW_004624745:22,816,292...22,861,613 		JBrowse link
G Cryzl1 crystallin zeta like 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,807,703...21,847,012
Ensembl chrNW_004624745:21,808,688...21,846,880 		JBrowse link
G Dnajc28 DnaJ heat shock protein family (Hsp40) member C28 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,715,732...21,720,373
Ensembl chrNW_004624745:21,717,745...21,718,902 		JBrowse link
G Donson DNA replication fork stabilization factor DONSON ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,798,712...21,807,657
Ensembl chrNW_004624745:21,798,075...21,807,556 		JBrowse link
G Epcip exosomal polycystin 1 interacting protein ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,031,717...21,064,616
Ensembl chrNW_004624745:21,034,962...21,035,675 		JBrowse link
G Eva1c eva-1 homolog C ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,746,101...20,835,142
Ensembl chrNW_004624745:20,747,018...20,835,259 		JBrowse link
G Gart phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,735,431...21,763,330
Ensembl chrNW_004624745:21,734,282...21,762,734 		JBrowse link
G Hunk hormonally up-regulated Neu-associated kinase ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,212,006...20,323,213
Ensembl chrNW_004624745:20,212,095...20,323,330 		JBrowse link
G Ifnar1 interferon alpha and beta receptor subunit 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,545,846...21,569,719
Ensembl chrNW_004624745:21,546,007...21,572,776 		JBrowse link
G Ifnar2 interferon alpha and beta receptor subunit 2 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,434,234...21,470,099
Ensembl chrNW_004624745:21,433,758...21,468,889 		JBrowse link
G Ifngr2 interferon gamma receptor 2 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,628,968...21,652,305
Ensembl chrNW_004624745:21,628,797...21,651,652 		JBrowse link
G Il10rb interleukin 10 receptor subunit beta ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,470,651...21,492,899
Ensembl chrNW_004624745:21,470,729...21,492,286 		JBrowse link
G Itsn1 intersectin 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,847,593...22,055,141
Ensembl chrNW_004624745:21,906,187...22,050,822 		JBrowse link
G Kcne1 potassium voltage-gated channel subfamily E regulatory subunit 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,624,414...22,631,625
Ensembl chrNW_004624745:22,624,765...22,631,609 		JBrowse link
G Kcne2 potassium voltage-gated channel subfamily E regulatory subunit 2 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,552,809...22,553,321
Ensembl chrNW_004624745:22,525,037...22,556,000 		JBrowse link
G Mis18a MIS18 kinetochore protein A ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,589,236...20,603,368
Ensembl chrNW_004624745:20,590,737...20,603,475 		JBrowse link
G Mrap melanocortin 2 receptor accessory protein ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,620,807...20,642,688 JBrowse link
G Mrps6 mitochondrial ribosomal protein S6 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,231,789...22,304,147
Ensembl chrNW_004624745:22,231,776...22,304,147 		JBrowse link
G Olig1 oligodendrocyte transcription factor 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,308,831...21,310,898
Ensembl chrNW_004624745:21,308,928...21,309,722 		JBrowse link
G Olig2 oligodendrocyte transcription factor 2 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,270,804...21,274,225
Ensembl chrNW_004624745:21,270,965...21,272,932 		JBrowse link
G Paxbp1 PAX3 and PAX7 binding protein 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,988,156...21,019,348
Ensembl chrNW_004624745:20,988,162...21,019,344 		JBrowse link
G Polg DNA polymerase gamma, catalytic subunit ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:18414213 PMID:21357833 PMID:21880868 PMID:25741868 PMID:26467025 More... NCBI chrNW_004624768:16,493,123...16,509,747
Ensembl chrNW_004624768:16,491,555...16,509,900 		JBrowse link
G Rcan1 regulator of calcineurin 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,683,600...22,764,735
Ensembl chrNW_004624745:22,683,016...22,764,720 		JBrowse link
G Scaf4 SR-related CTD associated factor 4 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,040,416...20,097,764
Ensembl chrNW_004624745:20,040,770...20,097,835 		JBrowse link
G Slc5a3 solute carrier family 5 member 3 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,231,434...22,264,555
Ensembl chrNW_004624745:22,231,887...22,258,965 		JBrowse link
G Smim11 small integral membrane protein 11 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:22,558,546...22,569,380
Ensembl chrNW_004624745:22,558,420...22,571,802 		JBrowse link
G Sod1 superoxide dismutase 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,032,003...20,037,958
Ensembl chrNW_004624745:20,032,011...20,037,958 		JBrowse link
G Son SON DNA and RNA binding protein ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,762,273...21,798,587
Ensembl chrNW_004624745:21,763,010...21,797,817 		JBrowse link
G Spg11 SPG11 vesicle trafficking associated, spatacsin ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:19105190 PMID:20110243 PMID:22154821 PMID:23733235 PMID:25741868 More... NCBI chrNW_004624804:11,569,024...11,672,037
Ensembl chrNW_004624804:11,569,150...11,670,373 		JBrowse link
G Synj1 synaptojanin 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 OMIM
ClinVar		 PMID:9536098 PMID:11413010 PMID:16199547 PMID:17576681 PMID:23804563 More... NCBI chrNW_004624745:20,881,312...20,984,242
Ensembl chrNW_004624745:20,881,317...20,984,184 		JBrowse link
G Tiam1 TIAM Rac1 associated GEF 1 ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:19,563,166...19,941,511
Ensembl chrNW_004624745:19,561,195...19,760,095 		JBrowse link
G Tmem50b transmembrane protein 50B ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:21,649,759...21,704,734
Ensembl chrNW_004624745:21,663,673...21,704,836 		JBrowse link
G Urb1 URB1 ribosome biogenesis homolog ISO ClinVar Annotator: match by term: Early-onset Parkinson disease 20 ClinVar PMID:28492532 NCBI chrNW_004624745:20,647,661...20,716,262
Ensembl chrNW_004624745:20,648,230...20,715,549 		JBrowse link
Parkinson's disease 21 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dnajc13 DnaJ heat shock protein family (Hsp40) member C13 ISO ClinVar Annotator: match by term: Parkinson disease 21 ClinVar PMID:24218364 PMID:25118025 PMID:27270108 PMID:28492532 NCBI chrNW_004624730:8,497,781...8,649,058
Ensembl chrNW_004624730:8,517,998...8,648,318 		JBrowse link
Parkinson's disease 22 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Chchd2 coiled-coil-helix-coiled-coil-helix domain containing 2 ISO ClinVar Annotator: match by term: Parkinson disease 22, autosomal dominant OMIM
ClinVar		 PMID:25662902 PMID:25741868 PMID:26067110 PMID:26067113 PMID:26561290 More... NCBI chrNW_004624740:8,279,416...8,283,730
Ensembl chrNW_004624740:8,278,078...8,283,657 		JBrowse link
Parkinson's disease 23 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Vps13c vacuolar protein sorting 13 homolog C ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 23 OMIM
ClinVar		 PMID:16199547 PMID:25741868 PMID:26942284 PMID:28492532 PMID:34875562 NCBI chrNW_004624781:10,259,971...10,414,421
Ensembl chrNW_004624781:10,259,976...10,413,278 		JBrowse link
Parkinson's disease 25 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ptpa protein phosphatase 2 phosphatase activator ISO ClinVar Annotator: match by term: Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development OMIM
ClinVar		 PMID:36073231 NCBI chrNW_004624760:5,974,881...6,001,975
Ensembl chrNW_004624760:5,974,881...6,001,979 		JBrowse link
Parkinson's Disease 26 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Rab32 RAB32, member RAS oncogene family susceptibility ISO OMIM NCBI chrNW_004624753:7,900,027...7,917,944
Ensembl chrNW_004624753:7,900,267...7,917,854 		JBrowse link
Parkinson's disease 4 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Snca synuclein alpha ISO ClinVar Annotator: match by term: Autosomal dominant Parkinson disease 4 OMIM
ClinVar		 PMID:11376188 PMID:21559878 PMID:25741868 PMID:26858591 PMID:28492532 More... NCBI chrNW_004624757:17,393,046...17,528,783
Ensembl chrNW_004624757:17,392,998...17,528,320 		JBrowse link
Parkinson's Disease 5 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Uchl1 ubiquitin C-terminal hydrolase L1 ISO ClinVar Annotator: match by term: Parkinson disease 5 | ClinVar Annotator: match by term: Parkinson disease 5, autosomal dominant, susceptibility to ClinVar
OMIM		 PMID:4514348 PMID:9774100 PMID:10203348 PMID:10563640 PMID:12408865 More... NCBI chrNW_004624761:25,786,028...25,797,641
Ensembl chrNW_004624761:25,784,257...25,797,549 		JBrowse link
Parkinson's disease 6 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aldh4a1 aldehyde dehydrogenase 4 family member A1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,051,999...4,081,954
Ensembl chrNW_004624764:4,051,178...4,082,142 		JBrowse link
G Alpl alkaline phosphatase, biomineralization associated ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,393,741...6,447,739
Ensembl chrNW_004624764:6,393,765...6,447,829 		JBrowse link
G C1qa complement C1q A chain ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:7,363,615...7,366,408
Ensembl chrNW_004624764:7,363,567...7,366,617 		JBrowse link
G C1qb complement C1q B chain ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:7,377,013...7,382,953
Ensembl chrNW_004624764:7,376,967...7,383,445 		JBrowse link
G C1qc complement C1q C chain ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:7,369,365...7,373,238
Ensembl chrNW_004624764:7,369,338...7,373,436 		JBrowse link
G Camk2n1 calcium/calmodulin dependent protein kinase II inhibitor 1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,544,589...5,547,811
Ensembl chrNW_004624764:5,544,484...5,547,683 		JBrowse link
G Capzb capping actin protein of muscle Z-line subunit beta ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,473,880...4,601,260
Ensembl chrNW_004624764:4,473,606...4,601,286 		JBrowse link
G Cda cytidine deaminase ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,621,888...5,645,055
Ensembl chrNW_004624764:5,621,899...5,645,850 		JBrowse link
G Cdc42 cell division cycle 42 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,874,453...6,891,952 JBrowse link
G Cela3b chymotrypsin like elastase 3B ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,773,548...6,781,998 JBrowse link
G Ddost dolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004624764:5,671,724...5,681,729
Ensembl chrNW_004624764:5,671,724...5,681,835 		JBrowse link
G Ece1 endothelin converting enzyme 1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,222,301...6,318,423
Ensembl chrNW_004624764:6,221,867...6,318,477 		JBrowse link
G Eif4g3 eukaryotic translation initiation factor 4 gamma 3 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,823,254...6,190,610
Ensembl chrNW_004624764:5,823,679...6,190,566 		JBrowse link
G Emc1 ER membrane protein complex subunit 1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,367,780...4,401,000
Ensembl chrNW_004624764:4,370,591...4,400,920 		JBrowse link
G Epha8 EPH receptor A8 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:7,307,967...7,339,187
Ensembl chrNW_004624764:7,307,967...7,339,169 		JBrowse link
G Fam43b family with sequence similarity 43 member B ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,594,388...5,597,088
Ensembl chrNW_004624764:5,595,133...5,596,125 		JBrowse link
G Hp1bp3 heterochromatin protein 1 binding protein 3 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,760,002...5,794,705 JBrowse link
G Hspg2 heparan sulfate proteoglycan 2 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,639,152...6,736,161
Ensembl chrNW_004624764:6,640,087...6,708,130 		JBrowse link
G Htr6 5-hydroxytryptamine receptor 6 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,778,563...4,791,505
Ensembl chrNW_004624764:4,778,657...4,791,458 		JBrowse link
G Iffo2 intermediate filament family orphan 2 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,083,495...4,128,307
Ensembl chrNW_004624764:4,086,119...4,127,948 		JBrowse link
G Kif17 kinesin family member 17 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,682,800...5,724,852
Ensembl chrNW_004624764:5,682,829...5,724,656 		JBrowse link
G Ldlrad2 low density lipoprotein receptor class A domain containing 2 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,631,231...6,639,010 JBrowse link
G Micos10 mitochondrial contact site and cristae organizing system subunit 10 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,709,978...4,749,620
Ensembl chrNW_004624764:4,710,105...4,744,769 		JBrowse link
G Mrto4 MRT4 homolog, ribosome maturation factor ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,401,005...4,406,157
Ensembl chrNW_004624764:4,400,731...4,407,180 		JBrowse link
G Mtfp1 mitochondrial fission process 1 ISO mRNA:decreased expression:brain (mouse) RGD PMID:19492057 RGD:12880394 NCBI chrNW_004624747:6,743,221...6,749,375
Ensembl chrNW_004624747:6,744,321...6,751,257 		JBrowse link
G Mul1 mitochondrial E3 ubiquitin protein ligase 1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,560,071...5,566,763
Ensembl chrNW_004624764:5,557,560...5,586,964 		JBrowse link
G Nbl1 NBL1, DAN family BMP antagonist ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,771,334...4,774,462
Ensembl chrNW_004624764:4,764,903...4,775,707 		JBrowse link
G Otud3 OTU deubiquitinase 3 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,950,727...4,979,856
Ensembl chrNW_004624764:4,949,975...4,976,067 		JBrowse link
G Park7 Parkinsonism associated deglycase ISO ClinVar Annotator: match by term: Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 ClinVar PMID:16632486 NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
G Pink1 PTEN induced kinase 1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 | ClinVar Annotator: match by term: PARKINSON DISEASE 6, EARLY-ONSET | ClinVar Annotator: match by term: PINK1-Related Parkinsonism | ClinVar Annotator: match by term: Parkinson disease 6 | ClinVar Annotator: match by term: Parkinson disease, autosomal recessive early-onset, digenic, PINK1/DJ1 OMIM
ClinVar		 PMID:2345993 PMID:9536098 PMID:15087508 PMID:15349860 PMID:15349870 More... NCBI chrNW_004624764:5,656,207...5,671,260
Ensembl chrNW_004624764:5,656,229...5,671,260 		JBrowse link
G Pla2g2a phospholipase A2 group IIA ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,144,549...5,152,517
Ensembl chrNW_004624764:5,144,549...5,151,995 		JBrowse link
G Pla2g2c phospholipase A2 group IIC ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,257,955...5,269,744 JBrowse link
G Pla2g2d phospholipase A2 group IID ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,224,071...5,229,603
Ensembl chrNW_004624764:5,224,018...5,229,609 		JBrowse link
G Pla2g2e phospholipase A2 group IIE ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,984,021...4,989,315
Ensembl chrNW_004624764:4,985,688...4,988,818 		JBrowse link
G Pla2g2f phospholipase A2 group IIF ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,243,507...5,249,842
Ensembl chrNW_004624764:5,244,152...5,249,842 		JBrowse link
G Pla2g5 phospholipase A2 group V ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,196,215...5,207,138
Ensembl chrNW_004624764:5,196,215...5,207,232 		JBrowse link
G Rap1gap RAP1 GTPase activating protein ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,460,230...6,521,693
Ensembl chrNW_004624764:6,460,230...6,506,741 		JBrowse link
G Rnf186 ring finger protein 186 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,897,234...4,898,470 JBrowse link
G Sh2d5 SH2 domain containing 5 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,726,245...5,737,755
Ensembl chrNW_004624764:5,724,776...5,733,244 		JBrowse link
G Slc66a1 solute carrier family 66 member 1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,455,843...4,466,413
Ensembl chrNW_004624764:4,457,156...4,465,109 		JBrowse link
G Tmco4 transmembrane and coiled-coil domains 4 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,793,324...4,882,334
Ensembl chrNW_004624764:4,793,812...4,882,266 		JBrowse link
G Ubr4 ubiquitin protein ligase E3 component n-recognin 4 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:4,223,784...4,358,923
Ensembl chrNW_004624764:4,223,784...4,358,885 		JBrowse link
G Ubxn10 UBX domain protein 10 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,277,390...5,285,508
Ensembl chrNW_004624764:5,277,398...5,285,499 		JBrowse link
G Usp48 ubiquitin specific peptidase 48 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,528,084...6,610,926 JBrowse link
G Vwa5b1 von Willebrand factor A domain containing 5B1 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:5,379,734...5,435,744
Ensembl chrNW_004624764:5,379,677...5,430,047 		JBrowse link
G Wnt4 Wnt family member 4 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:6,913,027...6,934,650
Ensembl chrNW_004624764:6,921,811...6,933,392 		JBrowse link
G Zbtb40 zinc finger and BTB domain containing 40 ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 6 ClinVar PMID:28492532 NCBI chrNW_004624764:7,198,964...7,268,544
Ensembl chrNW_004624764:7,198,213...7,275,021 		JBrowse link
Parkinson's disease 7 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Park7 Parkinsonism associated deglycase ISO ClinVar Annotator: match by term: Autosomal recessive early-onset Parkinson disease 7 OMIM
ClinVar		 PMID:1818649 PMID:9536098 PMID:12446870 PMID:12891675 PMID:12891685 More... NCBI chrNW_004624818:3,900,917...3,915,457
Ensembl chrNW_004624818:3,900,917...3,911,042 		JBrowse link
Parkinson's disease 8 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Lrrk2 leucine rich repeat kinase 2 ISO ClinVar Annotator: match by term: Autosomal dominant Parkinson disease 8 | ClinVar Annotator: match by term: LRRK2-related condition OMIM
ClinVar		 PMID:7898705 PMID:9276200 PMID:9536098 PMID:15541308 PMID:15541309 More... NCBI chrNW_004624778:106,594...279,325
Ensembl chrNW_004624778:108,761...279,230 		JBrowse link
Parkinson's Disease, Mitochondrial term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Fmc1 formation of mitochondrial complex V assembly factor 1 homolog ISO CTD Direct Evidence: marker/mechanism CTD PMID:29371327 NCBI chrNW_004624765:19,767,361...19,784,527
Ensembl chrNW_004624765:19,768,212...19,771,138 		JBrowse link
G Ndufv2 NADH:ubiquinone oxidoreductase core subunit V2 ISO ClinVar Annotator: match by term: Parkinson disease, mitochondrial ClinVar PMID:9570948 PMID:25741868 PMID:28492532 NCBI chrNW_004624770:17,925,250...17,950,754 JBrowse link
Parkinson's Disease, X-Linked Dominant term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Rab39b RAB39B, member RAS oncogene family ISO ClinVar Annotator: match by term: Parkinson disease, X-linked dominant ClinVar PMID:26399558 NCBI chrNW_004624963:51,978...71,781
Ensembl chrNW_004624963:63,187...73,440 		JBrowse link
PARKINSONISM WITH POLYNEUROPATHY term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G LOC101719627 cytochrome b-c1 complex subunit 1, mitochondrial ISO ClinVar Annotator: match by term: Parkinsonism with polyneuropathy OMIM
ClinVar		 PMID:25741868 PMID:33141179 NCBI chrNW_004624730:2,603,301...2,613,105
Ensembl chrNW_004624730:2,603,089...2,613,828 		JBrowse link
Parkinsonism-Dystonia, Childhood-Onset, 3 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Wars2 tryptophanyl tRNA synthetase 2, mitochondrial ISO ClinVar Annotator: match by term: Parkinsonism-dystonia 3, childhood-onset OMIM
ClinVar		 PMID:25741868 PMID:28236339 PMID:28492532 PMID:28905505 PMID:29120065 More... NCBI chrNW_004624772:14,652,874...14,735,732
Ensembl chrNW_004624772:14,654,403...14,735,315 		JBrowse link
Perry syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dctn1 dynactin subunit 1 ISO ClinVar Annotator: match by term: Parkinsonism with alveolar hypoventilation and mental depression | ClinVar Annotator: match by term: Perry syndrome ClinVar
OMIM		 PMID:12062019 PMID:12627231 PMID:15326253 PMID:16199547 PMID:16240349 More... NCBI chrNW_004624749:29,105,310...29,135,124
Ensembl chrNW_004624749:29,115,561...29,137,276 		JBrowse link
Progressive Supranuclear Palsy Atypical term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Mapt microtubule associated protein tau ISO ClinVar Annotator: match by term: Atypical PSP | ClinVar Annotator: match by term: Parkinson-dementia syndrome | ClinVar Annotator: match by term: Supranuclear palsy, progressive, 1, atypical ClinVar
OMIM		 PMID:2273997 PMID:7783864 PMID:7936288 PMID:8673924 PMID:8940276 More... NCBI chrNW_004624849:2,320,887...2,421,099 JBrowse link
secondary Parkinson disease term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp13a2 ATPase cation transporting 13A2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:22285144 NCBI chrNW_004624764:2,614,541...2,631,972
Ensembl chrNW_004624764:2,614,827...2,631,793 		JBrowse link
G Bche butyrylcholinesterase ISO CTD Direct Evidence: marker/mechanism CTD PMID:30410011 NCBI chrNW_004624730:43,793,550...43,849,169
Ensembl chrNW_004624730:43,793,040...43,843,519 		JBrowse link
G Cnr2 cannabinoid receptor 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:27317300 NCBI chrNW_004624764:8,388,375...8,422,961
Ensembl chrNW_004624764:8,389,444...8,390,538 		JBrowse link
G Fmc1 formation of mitochondrial complex V assembly factor 1 homolog ISO CTD Direct Evidence: marker/mechanism CTD PMID:29371327 NCBI chrNW_004624765:19,767,361...19,784,527
Ensembl chrNW_004624765:19,768,212...19,771,138 		JBrowse link
G Gdnf glial cell derived neurotrophic factor ISO CTD Direct Evidence: therapeutic CTD PMID:19909981 NCBI chrNW_004624759:17,263,570...17,290,046
Ensembl chrNW_004624759:17,263,969...17,287,723 		JBrowse link
G Nos2 nitric oxide synthase 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:25634431 NCBI chrNW_004624786:491,944...530,427
Ensembl chrNW_004624786:489,311...528,271 		JBrowse link
G Pon1 paraoxonase 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:26457621 NCBI chrNW_004624813:1,953,796...1,979,846
Ensembl chrNW_004624813:1,949,614...1,979,882 		JBrowse link
G Prkn parkin RBR E3 ubiquitin protein ligase ISO CTD Direct Evidence: marker/mechanism CTD PMID:15993444 NCBI chrNW_004624855:430,148...1,992,121
Ensembl chrNW_004624855:430,260...1,989,747 		JBrowse link
G Rgs2 regulator of G protein signaling 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:18347610 NCBI chrNW_004624814:754,743...758,148
Ensembl chrNW_004624814:753,164...758,192 		JBrowse link
G Shh sonic hedgehog signaling molecule ISO CTD Direct Evidence: therapeutic CTD PMID:11771942 NCBI chrNW_004624800:2,202,986...2,215,309
Ensembl chrNW_004624800:2,203,393...2,212,068 		JBrowse link
G Slc18a2 solute carrier family 18 member A2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:34774656 NCBI chrNW_004624737:29,356,590...29,388,099
Ensembl chrNW_004624737:29,358,696...29,387,808 		JBrowse link
G Snca synuclein alpha ISO CTD Direct Evidence: marker/mechanism CTD PMID:34332006 NCBI chrNW_004624757:17,393,046...17,528,783
Ensembl chrNW_004624757:17,392,998...17,528,320 		JBrowse link
G Tfam transcription factor A, mitochondrial ISO CTD Direct Evidence: marker/mechanism CTD PMID:28595911 NCBI chrNW_004624791:5,183,276...5,198,986
Ensembl chrNW_004624791:5,179,195...5,198,611 		JBrowse link
Waisman syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Clic2 chloride intracellular channel 2 ISO ClinVar Annotator: match by term: Early-onset parkinsonism-intellectual disability syndrome ClinVar PMID:25434005 NCBI chrNW_004624963:21,115...47,757 JBrowse link
G Rab39b RAB39B, member RAS oncogene family ISO ClinVar Annotator: match by term: Basal ganglia disorder with mental retardation | ClinVar Annotator: match by term: Early-onset parkinsonism-intellectual disability syndrome OMIM
ClinVar		 PMID:1674730 PMID:4025396 PMID:25434005 PMID:25741868 PMID:26399558 More... NCBI chrNW_004624963:51,978...71,781
Ensembl chrNW_004624963:63,187...73,440 		JBrowse link
X-linked parkinsonism-spasticity syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atp6ap2 ATPase H+ transporting accessory protein 2 ISO ClinVar Annotator: match by term: Parkinsonism with spasticity, X-linked | ClinVar Annotator: match by term: X-linked parkinsonism-spasticity syndrome OMIM
ClinVar		 PMID:20629132 PMID:23595882 PMID:25741868 PMID:26467025 PMID:28492532 NCBI chrNW_004624762:14,952,313...14,975,678
Ensembl chrNW_004624762:14,952,002...14,975,900 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14208
    disease of anatomical entity 13924
      nervous system disease 12254
        central nervous system disease 10972
          movement disease 2376
            Parkinsonism 401
              Dementia/Parkinsonism with Non-Alzheimer Amyloid Plaques 0
              Lewy body dementia + 40
              PARKINSONISM WITH POLYNEUROPATHY 1
              Parkinson's disease + 321
              Perry syndrome 1
              X-linked parkinsonism-spasticity syndrome 1
              secondary Parkinson disease + 17
              vascular Parkinsonism 0
Path 2
Term Annotations click to browse term
  disease 14208
    disease of anatomical entity 13924
      nervous system disease 12254
        central nervous system disease 10972
          brain disease 10297
            movement disease 2376
              Parkinsonism 401
                Dementia/Parkinsonism with Non-Alzheimer Amyloid Plaques 0
                Lewy body dementia + 40
                PARKINSONISM WITH POLYNEUROPATHY 1
                Parkinson's disease + 321
                Perry syndrome 1
                X-linked parkinsonism-spasticity syndrome 1
                secondary Parkinson disease + 17
                vascular Parkinsonism 0
paths to the root