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
CHP1	gene	CHP1	Expert Review Amber;Literature	Hereditary ataxia	Motor Disorders of the CNS	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Spastic ataxia 9, autosomal recessive, OMIM:618438				23904602;29379881;32787936		False	2	0;100;0	1.344	False		ENSG00000187446	ENSG00000187446	HGNC:17433													
COG5	gene	COG5	Expert Review Amber;Literature	Hereditary ataxia	Motor Disorders of the CNS	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	"Congenital disorder of glycosylation, type IIi	613612"				19690088;28960046		False	2	0;0;0	1.344	False		ENSG00000164597	ENSG00000164597	HGNC:14857													
EEF2	gene	EEF2	Expert Review Amber;Literature	Hereditary ataxia	Motor Disorders of the CNS	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Spinocerebellar ataxia 26 OMIM:609306				23001565;33355653		False	2	0;100;0	1.344	False		ENSG00000167658	ENSG00000167658	HGNC:3214													
MVK	gene	MVK	Expert Review Amber;Literature	Hereditary ataxia	Motor Disorders of the CNS	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Mevalonic aciduria, OMIM:610377				26503795;24896178		False	2	0;100;0	1.344	False		ENSG00000110921	ENSG00000110921	HGNC:7530													
POLR3K	gene	POLR3K	Expert Review Amber;Literature	Hereditary ataxia	Motor Disorders of the CNS	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Leukodystrophy, hypomyelinating, 21, OMIM:619310				30584594;33659930		False	2	0;100;0	1.344	False		ENSG00000161980	ENSG00000161980	HGNC:14121													
SAR1B	gene	SAR1B	Expert Review;Expert Review Amber	Hereditary ataxia	Motor Disorders of the CNS	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	"	Chylomicron retention disease	246700"						False	2	100;0;0	1.344	False		ENSG00000152700	ENSG00000152700	HGNC:10535													
VAMP1	gene	VAMP1	Expert Review Amber;Radboud University Medical Center, Nijmegen;UKGTN	Hereditary ataxia	Motor Disorders of the CNS	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Spastic ataxia 1, autosomal dominant, 108600						False	2	50;50;0	1.344	True		ENSG00000139190	ENSG00000139190	HGNC:12642