Mercurial > repos > nathandunn > monarchinitiative
diff test-data/genes-for-2-diseases.tsv @ 7:61d8060bf2ed draft
planemo upload commit cc498cdcd54060998f80018b8f2dc92345adc414
| author | nathandunn |
|---|---|
| date | Mon, 22 Aug 2016 12:41:24 -0400 |
| parents | 850bb90bd667 |
| children | 5fa1f0ca69cc |
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--- a/test-data/genes-for-2-diseases.tsv Wed Jun 29 14:17:39 2016 -0400 +++ b/test-data/genes-for-2-diseases.tsv Mon Aug 22 12:41:24 2016 -0400 @@ -1,136 +1,127 @@ -NCBIGene:37853 Mlp60A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:55737 VPS35 NCBITaxon:9606 Homo sapiens OMIM:614203 Parkinson Disease 17 ECO:0000220 sequencing assay evidence PMID:21763483|PMID:18342564|PMID:22991136|PMID:22517097|PMID:22801713 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:3313 HSPA9 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16565515 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:55532 SLC30A10 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:135138 PACRG NCBITaxon:9606 Homo sapiens OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile PMID:16328510 http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:3643 INSR NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:56997 ADCK3 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 ECO:0000033 traceable author statement PMID:18319072 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:57107 PDSS2 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:120892 LRRK2 NCBITaxon:9606 Homo sapiens OMIM:607060 autosomal dominant Parkinson disease 8 ECO:0000220 sequencing assay evidence PMID:16533964|PMID:18704525|PMID:23075850|PMID:21115957|PMID:16728648|PMID:17353388|PMID:9276200|PMID:16003110|PMID:15680455|PMID:15541309|PMID:19020907|PMID:16311269|PMID:15541308|PMID:16003110|PMID:16436782|PMID:17050822|PMID:15929036|PMID:16436781|PMID:16269541|PMID:19020907|PMID:17215492|PMID:18591067|PMID:20008657|PMID:15852371|PMID:17060595|PMID:16401756|PMID:16966502|PMID:15541309|PMID:19667187|PMID:17938369|PMID:15541309|PMID:7898705|PMID:16533964|PMID:15811455|PMID:19283415|PMID:15732108|PMID:15680456|PMID:19308469|PMID:15880653|PMID:16321986|PMID:16157909|PMID:15541309|PMID:18981379|PMID:16240353|PMID:15541308|PMID:17060595|PMID:16269541|PMID:16960813|PMID:16145815|PMID:15680457|PMID:16172858|PMID:15726496 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:605543 Parkinson Disease 4, Autosomal Dominant ECO:0000220 sequencing assay evidence PMID:17251522|PMID:15159488|PMID:14593171|PMID:14755720|PMID:8285594 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:2747 GLUD2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset PMID:19826450 http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:57017 COQ9 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4128 MAOA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:3569 IL6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:31826 rdgA NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4803 NGF NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:120892 LRRK2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915575|PMID:20205471|PMID:25149416|PMID:23628791|PMID:22043175|PMID:23017109|PMID:19915576|PMID:17388990|PMID:23472874 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:5071 PARK2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred +NCBIGene:4137 MAPT NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177|PMID:19915575 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:616361 Parkinson disease 21 ECO:0000220 sequencing assay evidence PMID:24218364 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:55737 VPS35 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:32133 Hsc70-3 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4929 NR4A2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:54832 VPS13C NCBITaxon:9606 Homo sapiens UMLS:CN202824 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:1621 DBH NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:5071 PARK2 NCBITaxon:9606 Homo sapiens UMLS:CN202824 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:6888 TALDO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:1906 EDN1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:11315 PARK7 NCBITaxon:9606 Homo sapiens OMIM:606324 Parkinson disease 7 ECO:0000220 sequencing assay evidence PMID:16240358|PMID:12446870|PMID:22492997|PMID:12446870|PMID:15365989|PMID:23792957|PMID:12953260|PMID:20639397|PMID:22492997|PMID:20639397|PMID:12953260 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:38990 Cpr66D NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset ECO:0000220|ECO:0000033 sequencing assay evidence|traceable author statement PMID:24475098|PMID:16966503|PMID:15970950|PMID:21421046|PMID:15349870 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:25793 FBXO7 NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322|ECO:0000220|ECO:0000033 imported manually asserted information used in automatic assertion|sequencing assay evidence|traceable author statement PMID:18513678|PMID:19038853|PMID:25029497|PMID:19038853|PMID:19038853 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4137 MAPT NCBITaxon:9606 Homo sapiens UMLS:CN226961 Progressive supranuclear palsy-pure akinesia with gait freezing syndrome ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:44643 Cnx99A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:2941 GSTA4 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:11315 PARK7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000323 imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:2580 GAK NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:2944 GSTM1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:3630 INS NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:39002 Prm NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3630 insulin NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:2944 GSTM1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:37853 Mlp60A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens UMLS:CN202824 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:4137 MAPT NCBITaxon:9606 Homo sapiens OMIM:260540 Parkinson-Dementia Syndrome ECO:0000220|ECO:0000322 sequencing assay evidence|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:33824 Gpdh NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:260540 Parkinson-Dementia Syndrome ECO:0000220|ECO:0000322 sequencing assay evidence|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:53564 retinin NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:26281 FGF20 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6311 ATXN2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred +NCBIGene:6531 SLC6A3 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:9763484|PMID:19590691|PMID:16112329|PMID:16963468 http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:1565 CYP2D6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15174030|PMID:14991823 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3482 insulin like growth factor 2 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:27235 COQ2 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4842 nitric oxide synthase 1 (neuronal) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:26383258 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:5243 ATP binding cassette subfamily B member 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20558393 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15882845|PMID:19946270|PMID:25149416|PMID:22043175|PMID:16573651|PMID:12588799|PMID:22841634|PMID:24582596|PMID:15198987|PMID:17010972|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4129 MAOB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred -NCBIGene:23590 PDSS1 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:43497 Obp99b NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240112 Progressive supranuclear palsy - progressive non fluent aphasia ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred -NCBIGene:31826 rdgA NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred -NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915575|PMID:23628791|PMID:25149416|PMID:23017109|PMID:20205471|PMID:22043175|PMID:23472874|PMID:19915576|PMID:17388990 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:2244 FGB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6315 ATXN8OS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred -NCBIGene:2670 glial fibrillary acidic protein NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:57107 PDSS2 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:56997 ADCK3 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 ECO:0000033 traceable author statement PMID:18319072 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3569 interleukin 6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4128 MAOA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:57017 coenzyme Q9 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:2747 GLUD2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:4803 nerve growth factor (beta polypeptide) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:199 AIF1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168601 autosomal dominant Parkinson disease 1 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4287 ATXN3 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:203228 chromosome 9 open reading frame 72 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred -NCBIGene:4566 TRNK NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329|PMID:19590691|PMID:16963468|PMID:9763484 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6311 ATXN2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred -NCBIGene:53564 retinin NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:26281 fibroblast growth factor 20 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4217 MAP3K5 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21815648 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:3077 HFE NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16824219 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:613643 Parkinson disease 5 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:5420 PODXL NCBITaxon:9606 Homo sapiens OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile PMID:26864383 http://data.monarchinitiative.org/ttl/clinvar.ttl inferred NCBIGene:2203 FBP1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4217 mitogen-activated protein kinase kinase kinase 5 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21815648 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3077 HFE NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16824219 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:605543 Parkinson Disease 4, Autosomal Dominant ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:607060 autosomal dominant Parkinson disease 8 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4929 NR4A2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:55532 SLC30A10 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3313 HSPA9 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16565515 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177|PMID:19915575 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:3643 INSR NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:2950 glutathione S-transferase pi 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17190945|PMID:23721876 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens OMIM:606693 Kufor-Rakeb syndrome ECO:0000033|ECO:0000220|ECO:0000322|ECO:0000220 traceable author statement|sequencing assay evidence|imported manually asserted information used in automatic assertion|sequencing assay evidence PMID:22768177|PMID:22022275|PMID:22847264 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:1728 NQO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens OMIM:614203 Parkinson Disease 17 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23037695|PMID:20800516|PMID:17010972|PMID:25149416|PMID:20423725|PMID:22898350|PMID:22043175|PMID:23792957|PMID:15784737 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:26058 GRB10 interacting GYF protein 2 NCBITaxon:9606 Homo sapiens OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens OMIM:606693 Parkinson disease 9 ECO:0000322|ECO:0000220|ECO:0000220|ECO:0000033 imported manually asserted information used in automatic assertion|sequencing assay evidence|sequencing assay evidence|traceable author statement PMID:21724849|PMID:16964263|PMID:22388936|PMID:16964263|PMID:26633545|PMID:26633545|PMID:495089|PMID:20853184|PMID:21724849|PMID:16964263|PMID:22768177|PMID:22022275|PMID:21094623|PMID:17485642|PMID:22847264|PMID:21724849|PMID:20310007 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4137 MAPT NCBITaxon:9606 Homo sapiens UMLS:CN201681 Progressive supranuclear palsy-corticobasal syndrome ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:2950 GSTP1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17190945|PMID:23721876 http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:38508 Cpr64Aa NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:3162 HMOX1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20664293|PMID:12151787|PMID:22355530|PMID:17690948|PMID:25149416|PMID:12732244|PMID:21245015|PMID:25064009|PMID:11535288|PMID:18353766|PMID:22166454|PMID:20711177|PMID:17131421|PMID:12885775|PMID:18322262|PMID:21892157|PMID:22043175|PMID:22185909|PMID:15099020|PMID:14535945|PMID:19915575|PMID:18841091|PMID:19915576|PMID:22110584 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -MGI:1857323 Up NCBITaxon:10090 Mus musculus DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:51142 CHCHD2 NCBITaxon:9606 Homo sapiens OMIM:616710 Parkinson disease 22, autosomal dominant ECO:0000220 sequencing assay evidence PMID:26067113|PMID:26067113|PMID:26067113|PMID:25662902|PMID:25662902|PMID:25662902 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred +NCBIGene:26058 GIGYF2 NCBITaxon:9606 Homo sapiens OMIM:607688 Parkinson disease 11 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:11315 PARK7 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23037695|PMID:20800516|PMID:15784737|PMID:23792957|PMID:22898350|PMID:25149416|PMID:20423725|PMID:17010972|PMID:22043175 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168601 Parkinson disease 1 ECO:0000220 sequencing assay evidence PMID:20437567|PMID:23526723|PMID:17251522|PMID:18852448|PMID:24158904|PMID:9499430|PMID:18852445|PMID:9827625|PMID:14593171|PMID:16358335|PMID:18195271|PMID:10417297|PMID:9197268|PMID:20340137|PMID:24158909|PMID:9462735|PMID:19632874|PMID:17489854|PMID:15451224|PMID:9506559|PMID:15451225|PMID:23427326|PMID:11376188|PMID:14755720|PMID:18704525|PMID:17625105|PMID:11261505|PMID:18852449|PMID:24936070 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:43829 ATPsynbeta NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:32133 Hsc70-3 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:616361 Parkinson Disease 21 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6908 TATA-box binding protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6202 RPS8 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:1621 dopamine beta-hydroxylase (dopamine beta-monooxygenase) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:683 BST1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915576 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3480 insulin like growth factor 1 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred -NCBIGene:100129518 LOC100129518 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257|PMID:18353766|PMID:25279756 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6147 ribosomal protein L23a NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:4535 ND1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:43690 chp NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:38418 kst NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens OMIM:613135 Parkinsonism-Dystonia, Infantile ECO:0000322|ECO:0000220 imported manually asserted information used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3481 IGF2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4576 TRNT NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred -NCBIGene:1815 dopamine receptor D4 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:39826 fax NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +MGI:1857323 Up NCBITaxon:10090 Mus musculus DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915575|PMID:25064009|PMID:20664293|PMID:17131421|PMID:22043175|PMID:18841091|PMID:12732244|PMID:22355530|PMID:18353766|PMID:19915576|PMID:11535288|PMID:20711177|PMID:18322262|PMID:22110584|PMID:14535945|PMID:12151787|PMID:15099020|PMID:22166454|PMID:17690948|PMID:12885775|PMID:22185909|PMID:21245015|PMID:21892157|PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4566 TRNK NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson disease, mitochondrial PMID:8602753|PMID:7647790|PMID:9674814|PMID:1899320|PMID:1910341|PMID:8513395|PMID:1900002|PMID:17200493|PMID:1334369|PMID:8069655|PMID:1910259|PMID:1848674|PMID:8264702|PMID:10699170|PMID:8447321|PMID:2112427|PMID:9529371|PMID:8170567|PMID:20581069|PMID:1661776|PMID:1678125|PMID:1463005|PMID:1487239|PMID:1324294 http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:11315 PARK7 NCBITaxon:9606 Homo sapiens UMLS:CN202824 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:9627 SNCAIP NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:120892 LRRK2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset PMID:27111571 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:9829 DNAJC6 NCBITaxon:9606 Homo sapiens OMIM:615528 Parkinson Disease 19, Juvenile-Onset ECO:0000220 sequencing assay evidence PMID:22563501|PMID:24220513|PMID:23211418 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred NCBIGene:1571 CYP2E1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred -NCBIGene:9829 DnaJ heat shock protein family (Hsp40) member C6 NCBITaxon:9606 Homo sapiens OMIM:615528 Parkinson Disease 19, Juvenile-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred -NCBIGene:9627 synuclein alpha interacting protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20947659|PMID:25064009 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:7124 tumor necrosis factor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred NCBIGene:9045 RPL14 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:33721 Rtnl1 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240094 Progressive supranuclear palsy - pure akinesia with gait freezing ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred -NCBIGene:497258 BDNF-AS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:7124 TNF NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25064009|PMID:20947659 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:23590 PDSS1 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred +NCBIGene:4129 MAOB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:3480 IGF1R NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:683 BST1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915576 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4137 MAPT NCBITaxon:9606 Homo sapiens Orphanet:240112 Progressive supranuclear palsy-progressive non-fluent aphasia syndrome ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:43497 Obp99b NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:2670 GFAP NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred +NCBIGene:2244 FGB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:5071 PARK2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416|PMID:19946270|PMID:15198987|PMID:22043175|PMID:23628791|PMID:15882845|PMID:24582596|PMID:12588799|PMID:17010972|PMID:16573651|PMID:22841634 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:5243 ABCB1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20558393 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4842 NOS1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:26383258 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:27235 COQ2 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 ECO:0000220 sequencing assay evidence PMID:17855635|PMID:17332895|PMID:17374725|PMID:16400613|PMID:20495179|PMID:16116126|PMID:17855635|PMID:20495179|PMID:17855635 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:3482 IGF2R NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:100129518 LOC100129518 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766|PMID:17188257|PMID:25279756 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:5071 PARK2 NCBITaxon:9606 Homo sapiens OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile ECO:0000220 sequencing assay evidence PMID:12056932|PMID:7565830|PMID:15970950|PMID:11487568|PMID:7565830|PMID:15970950|PMID:11405814|PMID:9802278|PMID:10072423|PMID:9560156|PMID:12056932|PMID:9802278|PMID:16049031|PMID:16130111|PMID:16049031|PMID:10072423|PMID:9634531|PMID:10072423|PMID:9731209|PMID:10939576|PMID:11009195|PMID:9560156|PMID:16476817|PMID:16049031|PMID:12707457|PMID:16049031|PMID:10894217|PMID:14519684|PMID:11487568|PMID:11163284|PMID:16476817|PMID:16130111|PMID:11402119|PMID:9731209|PMID:10894217|PMID:16086186|PMID:16049031|PMID:12056932 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred +NCBIGene:199 AIF1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6202 RPS8 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6908 TBP NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:33883 Cpr NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:54822 TRPM7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000220|ECO:0000323 sequencing assay evidence|imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17010972|PMID:21366594|PMID:22043175|PMID:24374061|PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:1356 CP NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25758665|PMID:19159062 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:54840 APTX NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:3122 HLA-DRA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:8867 SYNJ1 NCBITaxon:9606 Homo sapiens OMIM:615530 Parkinson disease 20, early-onset ECO:0000220 sequencing assay evidence PMID:23804577|PMID:23804563 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred NCBIGene:4099 MAG NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:8867 SYNJ1 NCBITaxon:9606 Homo sapiens OMIM:615530 Parkinson Disease 20, Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:6128 ribosomal protein L6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:1981 eukaryotic translation initiation factor 4 gamma, 1 NCBITaxon:9606 Homo sapiens OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred -NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred -NCBIGene:8398 phospholipase A2 group VI NCBITaxon:9606 Homo sapiens OMIM:612953 Parkinson Disease 14, Autosomal Recessive ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:6571 solute carrier family 18 (vesicular monoamine transporter), member 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:25793 F-box protein 7 NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322|ECO:0000033|ECO:0000220 imported manually asserted information used in automatic assertion|traceable author statement|sequencing assay evidence PMID:25029497 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset ECO:0000033|ECO:0000220 traceable author statement|sequencing assay evidence PMID:24475098|PMID:21421046 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:3122 HLA-DRA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:2580 GAK NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000323 imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred -NCBIGene:44643 Cnx99A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:2941 GSTA4 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:33883 Cpr NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:4571 MT-TP NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred -NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240103 Progressive supranuclear palsy - corticobasal syndrome ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred -NCBIGene:6888 TALDO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:1906 endothelin 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:38990 Cpr66D NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:1356 ceruloplasmin (ferroxidase) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19159062|PMID:25758665 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:54840 aprataxin NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:54822 TRPM7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000220|ECO:0000323 sequencing assay evidence|imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred -NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:22043175|PMID:17010972|PMID:25149416|PMID:21366594|PMID:24374061 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4137 MAPT NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:33721 Rtnl1 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:39826 fax NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6571 SLC18A2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:8398 PLA2G6 NCBITaxon:9606 Homo sapiens OMIM:612953 Parkinson disease 14 ECO:0000220 sequencing assay evidence PMID:18981035|PMID:20938027|PMID:18570303|PMID:20886109|PMID:18570303|PMID:18570303|PMID:20938027|PMID:18981035|PMID:20938027|PMID:26633545|PMID:21700586 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred +NCBIGene:1981 EIF4G1 NCBITaxon:9606 Homo sapiens OMIM:614251 Parkinson disease 18 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred +NCBIGene:6128 RPL6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:38418 kst NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset PMID:24218364 http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:4535 ND1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset PMID:7624338 http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:43690 chp NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6147 RPL23A NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:100861548 PINK1-AS NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset PMID:18685134|PMID:15349871|PMID:15087508|PMID:15955953|PMID:15596610|PMID:15349870|PMID:18524835|PMID:18003639|PMID:15087508|PMID:15349870|PMID:16207731|PMID:15824318|PMID:16207731|PMID:17030667|PMID:18704525|PMID:16769864|PMID:15970950 http://data.monarchinitiative.org/ttl/clinvar.ttl inferred +NCBIGene:1815 DRD4 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:4576 TRNT NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson disease, mitochondrial http://data.monarchinitiative.org/ttl/kegg.ttl inferred +NCBIGene:3481 IGF2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred +NCBIGene:6531 SLC6A3 NCBITaxon:9606 Homo sapiens OMIM:613135 Parkinsonism-Dystonia, Infantile ECO:0000220|ECO:0000322 sequencing assay evidence|imported manually asserted information used in automatic assertion PMID:21112253|PMID:22279524|PMID:19478460|PMID:19478460|PMID:21112253|PMID:21112253 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred