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
ADRA2A	gene	ADRA2A	Expert Review Red;Genomics England PanelApp	Lipodystrophy_Lipoatrophy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Lipodystrophy, familial partial, type 8, OMIM #620679			Lipodystrophy;HP:0009125	27376152		False	1	0;0;100	1.42	True		ENSG00000150594	ENSG00000150594	HGNC:281													
AKT2	gene	AKT2	Expert Review Red;Literature	Lipodystrophy_Lipoatrophy		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	AKT2-related familial partial lipodystrophy MONDO:0019192			Lipodystrophy;HP:0009125	27408773;21979934		False	1	50;0;50	1.42	True		ENSG00000105221	ENSG00000105221	HGNC:392													
CIDEC	gene	CIDEC	Expert Review Red;Victorian Clinical Genetics Services	Lipodystrophy_Lipoatrophy		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Lipodystrophy, familial partial, type 5, MIM# 615238			Lipodystrophy;HP:0009125	20049731		False	1	0;0;100	1.42	True		ENSG00000187288	ENSG00000187288	HGNC:24229													
MCM7	gene	MCM7	Expert Review Red;Literature	Lipodystrophy_Lipoatrophy		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Syndromic disease, MONDO:0002254, MCM7-related;Meier-Gorlin syndrome;Microcephaly;Intellectual disability;Lipodystrophy;Adrenal insufficiency			Lipodystrophy;HP:0009125	33654309;34059554		False	1	0;0;100	1.42	True		ENSG00000166508	ENSG00000166508	HGNC:6950													
SUPT7L	gene	SUPT7L	Expert Review Red;Literature	Lipodystrophy_Lipoatrophy		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Fischer-Zirnsak progeroid syndrome, MIM# 621130			Lipodystrophy;HP:0009125	PMID: 38592547		False	1	0;0;100	1.42	True		ENSG00000119760	ENSG00000119760	HGNC:30632