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
COQ2	gene	COQ2	Expert list;Expert Review Red	Liver Failure_Paediatric		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	Coenzyme Q10 deficiency, primary, 1, MIM#607426			Liver failure;HP:0001399	17332895		False	1	0;0;100	1.25	True		ENSG00000173085	ENSG00000173085	HGNC:25223													
CYC1	gene	CYC1	Expert list;Expert Review Red	Liver Failure_Paediatric		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	"Mitochondrial complex III deficiency, nuclear type 6, MIM#	615453"			Liver failure;HP:0001399	23910460		False	1	0;0;100	1.25	True		ENSG00000179091	ENSG00000179091	HGNC:2579													
IL18BP	gene	IL18BP	Expert list;Expert Review Red	Liver Failure_Paediatric		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	"{?Hepatitis, fulminant viral, susceptibility to}	618549"			Liver failure;HP:0001399	31213488		False	1	0;0;100	1.25	True		ENSG00000137496	ENSG00000137496	HGNC:5987													
PTF1A	gene	PTF1A	Expert list;Expert Review Red	Liver Failure_Paediatric		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	"Pancreatic agenesis 2, MIM#	615935"			Liver failure;HP:0001399	24212882		False	1	0;0;100	1.25	True		ENSG00000168267	ENSG00000168267	HGNC:23734