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
UQCC1	gene	UQCC1	Expert Review Red;NHS GMS	Mitochondrial disorder with complex III deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	1	50;50;0	2.7	True		ENSG00000101019	ENSG00000101019	HGNC:15891													
UQCR10	gene	UQCR10	Expert Review Red;NHS GMS	Mitochondrial disorder with complex III deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	1	50;50;0	2.7	True		ENSG00000184076	ENSG00000184076	HGNC:30863													
UQCR11	gene	UQCR11	Expert Review Red;NHS GMS	Mitochondrial disorder with complex III deficiency		Mitochondrial	Unknown	No OMIM phenotype						False	1	50;50;0	2.7	True		ENSG00000127540	ENSG00000127540	HGNC:30862