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
PLIN1	gene	PLIN1	Expert Review Amber;Radboud University Medical Center, Nijmegen	Insulin resistance (including lipodystrophy)	Disorders of unusual phenotypes	Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Lipodystrophy, familial partial, type 4, 613877				25114292;21345103;30020498		False	2	100;0;0	1.18	False	Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments	ENSG00000166819	ENSG00000166819	HGNC:9076