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
UQCC3	gene	UQCC3	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex III deficiency		Mitochondrial	BIALLELIC, autosomal or pseudoautosomal	?Mitochondrial complex III deficiency, nuclear type 9, 616111				25008109		False	2	67;33;0	2.7	True		ENSG00000204922	ENSG00000204922	HGNC:34399													
UQCRC1	gene	UQCRC1	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex III deficiency		Mitochondrial	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinsonism with polyneuropathy, OMIM:619279				30788857;33141179;33779694;33248804		False	2	25;75;0	2.7	True		ENSG00000010256	ENSG00000010256	HGNC:12585													
UQCRH	gene	UQCRH	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex III deficiency		Mitochondrial	BIALLELIC, autosomal or pseudoautosomal	No OMIM phenotype						False	2	33;67;0	2.7	True		ENSG00000173660	ENSG00000173660	HGNC:12590													
UQCRQ	gene	UQCRQ	Expert Review Amber;NHS GMS	Mitochondrial disorder with complex III deficiency		Mitochondrial	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial complex III deficiency, nuclear type 4, 615159				18439546		False	2	67;33;0	2.7	True		ENSG00000164405	ENSG00000164405	HGNC:29594