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
GNAL	gene	GNAL	Expert list;Expert Review Amber	Complex Parkinsonism (includes pallido-pyramidal syndromes)	Neurodegenerative disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	 Dystonia 25, 615073				http://www.ncbi.nlm.nih.gov/books/NBK1155/;27222887;27123488;27093447;26810727;26725140;26506956;26365774;25847575;25382112		False	2	0;0;100	0.55	False		ENSG00000141404	ENSG00000141404	HGNC:4388													
HTRA2	gene	HTRA2	Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen	Complex Parkinsonism (includes pallido-pyramidal syndromes)	Neurodegenerative disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Parkinson disease 13, 610297;Parkinson Disease, Dominant						False	2	0;0;0	0.55	False		ENSG00000115317	ENSG00000115317	HGNC:14348													
TAF1	gene	TAF1	Expert Review Amber;Radboud University Medical Center, Nijmegen	Complex Parkinsonism (includes pallido-pyramidal syndromes)	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						False	2	0;0;0	0.55	False		ENSG00000147133	ENSG00000147133	HGNC:11535