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
ATP1A4	gene	ATP1A4	Expert Review Red;Literature	Alternating Hemiplegia and Hemiplegic Migraine		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hemiplegic migraine				32549268		False	1	0;0;100	0.57	True		ENSG00000132681	ENSG00000132681	HGNC:14073													
PNKD	gene	PNKD	Expert Review Red;Victorian Clinical Genetics Services	Alternating Hemiplegia and Hemiplegic Migraine		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paroxysmal nonkinesigenic dyskinesia 1, MIM# 118800						False	1	0;0;100	0.57	True		ENSG00000127838	ENSG00000127838	HGNC:9153