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
ACTB	gene	ACTB	Expert Review Green;South West GLH	GMS Neurology specialist test group-Movement disorders - childhood onset-SWGLH			MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Dystonia, juvenile-onset, 607371Baraitser-Winter syndrome 1, 243310						False	3	100;0;0	0.12	False		ENSG00000075624	ENSG00000075624	HGNC:132													
GNAL	gene	GNAL	Expert Review Green;South West GLH	GMS Neurology specialist test group-Movement disorders - childhood onset-SWGLH			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dystonia 25, 615073						False	3	100;0;0	0.12	False		ENSG00000141404	ENSG00000141404	HGNC:4388													
NKX2-1	gene	NKX2-1	Expert Review Green;South West GLH	GMS Neurology specialist test group-Movement disorders - childhood onset-SWGLH			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Chorea, hereditary benign 118700;Choreoathetosis, hypothyroidism, and neonatal respiratory distress 610978						False	3	100;0;0	0.12	False		ENSG00000136352	ENSG00000136352	HGNC:11825													
SUOX	gene	SUOX	Expert Review Green;South West GLH	GMS Neurology specialist test group-Movement disorders - childhood onset-SWGLH			BIALLELIC, autosomal or pseudoautosomal	Sulfite oxidase deficiency, 272300						False	3	100;0;0	0.12	False		ENSG00000139531	ENSG00000139531	HGNC:11460