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
DNAL4	gene	DNAL4	Other	Mirror movements		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Mirror movements 3 MIM#616059				25098561;25236653		False	1	0;0;100	1.1	False		ENSG00000100246	ENSG00000100246	HGNC:2955													
RBM15	gene	RBM15	Expert Review Red;Literature	Mirror movements		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Congenital mirror movements, RBM15-related, MONDO:0016558				41058181		False	1	0;0;100	1.1	True		ENSG00000162775	ENSG00000162775	HGNC:14959