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
AGPS	gene	AGPS	Expert Review Red	Monogenic diabetes		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	Lipodystrophy, congenital generalized, type 1, 608594						False	1	0;0;0	3.22	False		ENSG00000018510	ENSG00000018510	HGNC:327													
CAV1	gene	CAV1	Expert Review Red	Monogenic diabetes		Endocrinology	Unknown	Lipodystrophy, congenital generalized, type 3, 612526;Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome				18211975		False	1	0;0;0	3.22	False		ENSG00000105974	ENSG00000105974	HGNC:1527													
CIDEC	gene	CIDEC	Expert Review Red	Monogenic diabetes		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	Lipodystrophy, familial partial, type 5				20049731		False	1	0;0;0	3.22	False		ENSG00000187288	ENSG00000187288	HGNC:24229