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
ALS2	gene	ALS2	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000003393	ENSG00000003393	HGNC:443													
ANG	gene	ANG	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000214274	ENSG00000214274	HGNC:483													
ATP7B	gene	ATP7B	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000123191	ENSG00000123191	HGNC:870													
FA2H	gene	FA2H	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 35, autosomal recessive, MIM# 612319			Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000103089	ENSG00000103089	HGNC:21197													
FIG4	gene	FIG4	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000112367	ENSG00000112367	HGNC:16873													
GCH1	gene	GCH1	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000131979	ENSG00000131979	HGNC:4193													
GSN	gene	GSN	Expert list;Expert Review Red	Early-onset Dementia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyloidosis, Finnish type MIM#105120			Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000148180	ENSG00000148180	HGNC:4620													
HTRA2	gene	HTRA2	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000115317	ENSG00000115317	HGNC:14348													
NR4A2	gene	NR4A2	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	True		ENSG00000153234	ENSG00000153234	HGNC:7981													
PPIA	gene	PPIA	Expert Review Red;Literature	Early-onset Dementia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	amyotrophic lateral sclerosis, MONDO:0004976, PPIA-associated			Cognitive impairment;HP:0100543	34972208		False	1	0;0;100	1.29	True		ENSG00000196262	ENSG00000196262	HGNC:9253													
SETX	gene	SETX	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	False		ENSG00000107290	ENSG00000107290	HGNC:445													
SNCB	gene	SNCB	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dementia, Lewy body, MIM#127750			Cognitive impairment;HP:0100543	15365127;20697047		False	1	0;0;100	1.29	True		ENSG00000074317	ENSG00000074317	HGNC:11140													
SOD1	gene	SOD1	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	False		ENSG00000142168	ENSG00000142168	HGNC:11179													
SPART	gene	SPART	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	False		ENSG00000133104	ENSG00000133104	HGNC:18514													
TET2	gene	TET2	Expert Review Red;Literature	Early-onset Dementia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dementia			Cognitive impairment;HP:0100543	32330418;31943063		False	1	0;0;100	1.29	True		ENSG00000168769	ENSG00000168769	HGNC:25941													
TH	gene	TH	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	False		ENSG00000180176	ENSG00000180176	HGNC:11782													
UCHL1	gene	UCHL1	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown				Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	False		ENSG00000154277	ENSG00000154277	HGNC:12513													
VAPB	gene	VAPB	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Early-onset Dementia		Neurology and neurodevelopmental disorders	Unknown	Amyotrophic lateral sclerosis 8 MIM#608627;Spinal muscular atrophy, late-onset, Finkel type MIM#182980			Cognitive impairment;HP:0100543			False	1	0;0;100	1.29	False		ENSG00000124164	ENSG00000124164	HGNC:12649