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
B3GNT2	gene	B3GNT2	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Red;Victorian Clinical Genetics Services	Lissencephaly and Band Heterotopia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Muscular dystrophy-dystroglycanopathy				23359570;23877401		False	1	0;0;100	1.21	True		ENSG00000170340	ENSG00000170340	HGNC:15629													
BICD2	gene	BICD2	Expert Review Red;Literature	Lissencephaly and Band Heterotopia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder (MONDO#0700092), BICD2-related				35896821		False	1	0;0;100	1.21	True		ENSG00000185963	ENSG00000185963	HGNC:17208													
CLASP1	gene	CLASP1	Expert Review Red;Literature	Lissencephaly and Band Heterotopia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	neurodevelopmental disorder MONDO:0700092, CLASP1-related				39040917		False	1	0;0;100	1.21	True		ENSG00000074054	ENSG00000074054	HGNC:17088													
SRD5A3	gene	SRD5A3	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Red;Victorian Clinical Genetics Services	Lissencephaly and Band Heterotopia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type Iq (MIM#612379)				18271001;20637498;31638560;27480077		False	1	0;0;100	1.21	True		ENSG00000128039	ENSG00000128039	HGNC:25812													
