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
APP	gene	APP	Expert list;Expert Review Green	Cerebral amyloid angiopathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cerebral amyloid angiopathy, APP-related MONDO:0011583			Cerebral amyloid angiopathy;HP:0011970	16178030;11409420;16612981;19225789		False	3	100;0;0	1.1	True	Other	ENSG00000142192	ENSG00000142192	HGNC:620													
CST3	gene	CST3	Expert list;Expert Review Green	Cerebral amyloid angiopathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cerebral amyloid angiopathy MIM#105150			Cerebral amyloid angiopathy;HP:0011970	22435454;8866434;2602413;8108423		False	3	100;0;0	1.1	True	Other	ENSG00000101439	ENSG00000101439	HGNC:2475													
ITM2B	gene	ITM2B	Expert list;Expert Review Green	Cerebral amyloid angiopathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cerebral amyloid angiopathy MONDO:0005620			Cerebral amyloid angiopathy;HP:0011970	10391242;10781099;20385796;33814452		False	3	100;0;0	1.1	True	Other	ENSG00000136156	ENSG00000136156	HGNC:6174													
PRNP	gene	PRNP	Expert Review Green;Literature	Cerebral amyloid angiopathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	PrP systemic amyloidosis MONDO:0018339			Cerebral amyloid angiopathy;HP:0011970	8570627;19225789;34128081;19911184;24224623		False	3	100;0;0	1.1	False	Other	ENSG00000171867	ENSG00000171867	HGNC:9449													
PSEN1	gene	PSEN1	Expert Review Green;Literature	Cerebral amyloid angiopathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	cerebral amyloid angiopathy MONDO:0005620			Cerebral amyloid angiopathy;HP:0011970	11701593;11079548;34319632		False	3	100;0;0	1.1	True	Other	ENSG00000080815	ENSG00000080815	HGNC:9508													
TTR	gene	TTR	Expert Review Green;Literature	Cerebral amyloid angiopathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	cerebral amyloid angiopathy MONDO:0005620			Cerebral amyloid angiopathy;HP:0011970	35040071;8579098;31257920;27466465;28991667;11422811		False	3	100;0;0	1.1	True	Other	ENSG00000118271	ENSG00000118271	HGNC:12405													
PSEN2	gene	PSEN2	Expert Review Amber;Literature	Cerebral amyloid angiopathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	cerebral amyloid angiopathy MONDO:0005620			Cerebral amyloid angiopathy;HP:0011970	9450781;26888304		False	2	0;100;0	1.1	True	Other	ENSG00000143801	ENSG00000143801	HGNC:9509