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
MT-ND1	gene	MT-ND1	Expert List;Expert Review Green	Leber hereditary optic neuropathy		Mitochondrial	MITOCHONDRIAL	Leber's hereditary optic neuropathy;External ophthalmoplegia;Optic neuropathy and nystagmus				26448634;24884847;27449621;23665487;24800637;27177320;20301353		False	3	100;0;0	2.10	False		ENSG00000198888	ENSG00000198888	HGNC:7455													
MT-ND4	gene	MT-ND4	Expert List;Expert Review Green	Leber hereditary optic neuropathy		Mitochondrial	MITOCHONDRIAL	Leber's hereditary optic neuropathy				26448634;27159682;23665487;23805034;26683077;22553750;20301353		False	3	100;0;0	2.10	False		ENSG00000198886	ENSG00000198886	HGNC:7459													
MT-ND6	gene	MT-ND6	Expert List;Expert Review Green	Leber hereditary optic neuropathy		Mitochondrial	MITOCHONDRIAL	severe infantile-onset complex I deficiency;Nystagmus;Leber hereditary optic neuropathy				26448634;24884847;24398099;24417559;35567411		False	3	100;0;0	2.10	False		ENSG00000198695	ENSG00000198695	HGNC:7462