Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
ARSA	gene	ARSA	Expert list;Expert Review Amber	Parkinson Disease and Complex Parkinsonism	Neurodegenerative disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Metachromatic leukodystrophy, OMIM:250100;metachromatic leukodystrophy, juvenile form, MONDO:0009591				37381728;31312839		False	2	0;100;0	1.128	False		ENSG00000100299	ENSG00000100299	HGNC:713													
CHCHD2	gene	CHCHD2	Expert Review Amber;Literature	Parkinson Disease and Complex Parkinsonism	Neurodegenerative disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinson disease 22, autosomal dominant;616710				Funayama, M., Ohe, K., Amo, T., Furuya, N., Yamaguchi, J., Saiki, S., Li, Y., Ogaki, K., Ando, M., Yoshino, H., Tomiyama, H., Nishioka, K., and 12 others. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study. Lancet Neurol. 14: 274-282, 2015;26067114;25662902;26067110		False	2	33;33;33	1.128	False		ENSG00000106153	ENSG00000106153	HGNC:21645													
COASY	gene	COASY	Expert list;Expert Review Amber	Parkinson Disease and Complex Parkinsonism	Neurodegenerative disorders	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Neurodegeneration with brain iron accumulation 6, OMIM:615643;neurodegeneration with brain iron accumulation 6, MONDO:0014290				11980892;25778941;24360804;27021474;28489334;30089828;36495139		False	2	0;100;0	1.128	False		ENSG00000068120	ENSG00000068120	HGNC:29932													
TAF1	gene	TAF1	Expert Review Amber;Radboud University Medical Center, Nijmegen	Parkinson Disease and Complex Parkinsonism	Neurodegenerative disorders	Neurology and neurodevelopmental disorders	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Dystonia-Parkinsonism, X-linked, 314250;SVA retrotransposon insertion Dystonia-Parkinsonism, X-linked, 314250				17273961;17668393;26637982;20301662;12928496		False	2	100;0;0	1.128	False	Other - please provide details in the comments	ENSG00000147133	ENSG00000147133	HGNC:11535