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
ERMARD	gene	ERMARD	Australian Genomics Health Alliance Brain Malformation Flagship;Expert Review Red;Victorian Clinical Genetics Services	Periventricular Grey Matter Heterotopia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Periventricular nodular heterotopia 6, MIM#615544			Grey matter heterotopia;HP:0002282	24056535;27087860		False	1	0;0;100	1.2	True		ENSG00000130023	ENSG00000130023	HGNC:21056													
SYNCRIP	gene	SYNCRIP	Expert Review Red;Literature	Periventricular Grey Matter Heterotopia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	SYNCRIP-related neurodevelopmental disorder			Grey matter heterotopia;HP:0002282	34157790		False	1	0;0;100	1.2	True		ENSG00000135316	ENSG00000135316	HGNC:16918													
TMTC3	gene	TMTC3	Expert Review Red;Literature	Periventricular Grey Matter Heterotopia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Lissencephaly 8 (MIM#617255)			Grey matter heterotopia;HP:0002282	27773428;28973161		False	1	0;0;100	1.2	True		ENSG00000139324	ENSG00000139324	HGNC:26899