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
DMXL2	gene	DMXL2	Expert Review Amber;Other	Diabetes with additional phenotypes suggestive of a monogenic aetiology	Disorders of unusual phenotypes	Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sensorineural Hearing Loss;ORPHA90636;OMIM:612186				27657680;22875945;25248098		False	2	0;0;0	1.69	False		ENSG00000104093	ENSG00000104093	HGNC:2938													
PLIN1	gene	PLIN1	Expert Review;Expert Review Amber	Diabetes with additional phenotypes suggestive of a monogenic aetiology	Disorders of unusual phenotypes	Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	partial lipodystrophy, severe dyslipidemia, and insulin-resistant diabetes 				21345103;30020498		False	2	100;0;0	1.69	True		ENSG00000166819	ENSG00000166819	HGNC:9076