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
DNMT1	gene	DNMT1	Emory Genetics Laboratory;Expert Review Green;Illumina TruGenome Clinical Sequencing Services;Radboud University Medical Center, Nijmegen;UKGTN	Kleine-Levin syndrome	Sleep disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Neuropathy, hereditary sensory, type IE, 614116; Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant, 604121;CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN				22328086;24709307;23904686;31984424		False	3	0;0;0	1.8	False		ENSG00000130816	ENSG00000130816	HGNC:2976													
CSNK1D	gene	CSNK1D	Expert Review Amber;Radboud University Medical Center, Nijmegen	Kleine-Levin syndrome	Sleep disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Advanced sleep-phase syndrome, familial, 2, 615224				23636092;25660813		False	2	0;0;0	1.8	False		ENSG00000141551	ENSG00000141551	HGNC:2452													
MOG	gene	MOG	Expert Review Amber	Kleine-Levin syndrome	Sleep disorders	Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Narcolepsy 7, 614250				21907016		False	2	100;0;0	1.8	False		ENSG00000204655	ENSG00000204655	HGNC:7197