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
CTNND2	gene	CTNND2	Expert Review Amber;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual disability;Autism;Epilepsy			Autism;HP:0000717	25839933;29127138;25807484		False	2	0;100;0	0.205	True		ENSG00000169862	ENSG00000169862	HGNC:2516													
KATNAL2	gene	KATNAL2	Expert Review Amber;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Autism			Autism;HP:0000717	22495311;21572417;22495309;22495306		False	2	0;100;0	0.205	True		ENSG00000167216	ENSG00000167216	HGNC:25387													
TAOK2	gene	TAOK2	Expert Review Amber;Literature	Autism		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Autism			Autism;HP:0000717	29467497		False	2	0;100;0	0.205	True		ENSG00000149930	ENSG00000149930	HGNC:16835