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
AGRP	gene	AGRP	Expert Review Red;Victorian Clinical Genetics Services	Severe early-onset obesity		Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Leanness, inherited} 601665;{Obesity, late-onset} 601665;Obesity disorder, MONDO:0011122, AGRP-related			Obesity;HP:0001513	41680086		False	1	0;0;100	1.32	True		ENSG00000159723	ENSG00000159723	HGNC:330													
AKR1C2	gene	AKR1C2	Expert Review Red;Genomics England PanelApp	Severe early-onset obesity		Endocrine disorders	Unknown	Obesity			Obesity;HP:0001513	33675863;25322899		False	1	0;0;100	1.32	True		ENSG00000151632	ENSG00000151632	HGNC:385													
KSR2	gene	KSR2	Expert Review Red;Genomics England PanelApp	Severe early-onset obesity		Endocrine disorders	Other	obesity			Obesity;HP:0001513	29273807		False	1	0;0;100	1.32	True		ENSG00000171435	ENSG00000171435	HGNC:18610													
NR0B2	gene	NR0B2	Expert Review Red;Genomics England PanelApp	Severe early-onset obesity		Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Obesity, mild, early-onset MIM#601665			Obesity;HP:0001513	11136233;15459958		False	1	0;0;100	1.32	True		ENSG00000131910	ENSG00000131910	HGNC:7961													
PPARG	gene	PPARG	Expert Review Red;Genomics England PanelApp	Severe early-onset obesity		Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Obesity, severe, MIM#601665			Obesity;HP:0001513	9425261;9753710		False	1	0;0;100	1.32	True		ENSG00000132170	ENSG00000132170	HGNC:9236													
TRIM32	gene	TRIM32	Expert Review Red;Genomics England PanelApp;Victorian Clinical Genetics Services	Severe early-onset obesity		Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 11, MIM# 615988			Obesity;HP:0001513	16606853		False	1	0;0;100	1.32	True		ENSG00000119401	ENSG00000119401	HGNC:16380													
WDPCP	gene	WDPCP	Expert Review Red;Genomics England PanelApp;Victorian Clinical Genetics Services	Severe early-onset obesity		Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 15, MIM# 615992			Obesity;HP:0001513	20671153;25427950		False	1	0;0;100	1.32	True		ENSG00000143951	ENSG00000143951	HGNC:28027