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
ANO1	gene	ANO1	Expert Review Amber;Literature	Stroke		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Moyamoya disease 7, MIM# 620687			Stroke;HP:0001297	PMID: 37253099		False	2	0;100;0	1.50	True		ENSG00000131620	ENSG00000131620	HGNC:21625													
CST3	gene	CST3	Expert Review Amber;Expert Review Green;Royal Melbourne Hospital	Stroke		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cerebral amyloid angiopathy, MIM# 105150			Stroke;HP:0001297	3495457		False	2	50;50;0	1.50	True		ENSG00000101439	ENSG00000101439	HGNC:2475													
FLNA	gene	FLNA	Expert Review Amber;Royal Melbourne Hospital	Stroke		Neurology and neurodevelopmental disorders	Other	Heterotopia, periventricular, 1 , MIM#300049;Melnick-Needles syndrome 30, MIM#9350			Stroke;HP:0001297	21031081		False	2	50;50;0	1.50	True		ENSG00000196924	ENSG00000196924	HGNC:3754													
FOXM1	gene	FOXM1	Expert Review Amber;Literature	Stroke		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Moyamoya disease MONDO:0016820			Stroke;HP:0001297	38969938		False	2	0;100;0	1.50	True		ENSG00000111206	ENSG00000111206	HGNC:3818													
MT-TQ	gene	MT-TQ	Expert list;Expert Review Amber	Stroke		Neurology and neurodevelopmental disorders	MITOCHONDRIAL	Mitochondrial disease (MONDO:0044970), MT-TQ-related			Stroke;HP:0001297	11171912;10996779;17003408;11335700		False	2	0;100;0	1.50	True		ENSG00000210107	ENSG00000210107	HGNC:7495													
NOS3	gene	NOS3	Expert Review Amber;Royal Melbourne Hospital;Victorian Clinical Genetics Services	Stroke		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	{Ischemic stroke, susceptibility to} MIM#601367;Moyamoya disease, MONDO:0016820			Stroke;HP:0001297	24986538;28084234;36941667;37383439		False	2	0;25;75	1.50	True		ENSG00000164867	ENSG00000164867	HGNC:7876													
PTGIS	gene	PTGIS	Expert Review Amber;Literature	Stroke		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Vascular disorder, MONDO:0005385, PTGIS-related			Stroke;HP:0001297	42033196		False	2	0;100;0	1.50	True		ENSG00000124212	ENSG00000124212	HGNC:9603