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
DCC	gene	DCC	Expert list;Expert Review Green	Mirror movements		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Mirror movements 1 and/or agenesis of the corpus callosum MIM#157600				20431009;25763452;28250454		False	3	100;0;0	1.0	False		ENSG00000187323	ENSG00000187323	HGNC:2701													
NTN1	gene	NTN1	Expert list;Expert Review Green	Mirror movements		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Mirror movements 4 MIM#618264				25763452;28945198;33472083		False	3	100;0;0	1.0	True		ENSG00000065320	ENSG00000065320	HGNC:8029													
RAD51	gene	RAD51	Expert list;Expert Review Green	Mirror movements		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Mirror movements 2 MIM#614508				25763452;22305526;27830107;24808016		False	3	100;0;0	1.0	True		ENSG00000051180	ENSG00000051180	HGNC:9817													
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	1.0	False		ENSG00000100246	ENSG00000100246	HGNC:2955