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
ATP5B	gene	ATP5B	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex V deficiency		Mitochondrial	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	?Hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2, OMIM: 620085				36239646;36860166		False	2	25;75;0	3.3	True		ENSG00000110955	ENSG00000110955	HGNC:830													
ATP5C1	gene	ATP5C1	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex V deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	2	33;67;0	3.3	True		ENSG00000165629	ENSG00000165629	HGNC:833													
ATP5G1	gene	ATP5G1	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex V deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	2	33;67;0	3.3	True		ENSG00000159199	ENSG00000159199	HGNC:841													
ATP5G2	gene	ATP5G2	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex V deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	2	33;67;0	3.3	True		ENSG00000135390	ENSG00000135390	HGNC:842													
ATP5I	gene	ATP5I	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex V deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	2	33;67;0	3.3	True		ENSG00000169020	ENSG00000169020	HGNC:846													
ATP5J	gene	ATP5J	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex V deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	2	33;67;0	3.3	True		ENSG00000154723	ENSG00000154723	HGNC:847