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
ADA	gene	ADA	Expert Review Red;Literature	Autoinflammatory disorders		Immunology	BIALLELIC, autosomal or pseudoautosomal	Severe combined immunodeficiency due to ADA deficiency, OMIM:102700;Adenosine deaminase deficiency, partial, OMIM:102700				32098966		False	1	100;0;0	2.39	False		ENSG00000196839	ENSG00000196839	HGNC:186													
GP6	gene	GP6	Expert Review;Expert Review Red;Literature	Autoinflammatory disorders		Immunology	BIALLELIC, autosomal or pseudoautosomal	Bleeding disorder, platelet-type, 11, OMIM:614201				32098966		False	1	100;0;0	2.39	False		ENSG00000088053	ENSG00000088053	HGNC:14388													
SEC23B	gene	SEC23B	Expert Review Red;Literature	Autoinflammatory disorders		Immunology	BIALLELIC, autosomal or pseudoautosomal	Dyserythropoietic anemia, congenital, type II, OMIM:224100				32098966		False	1	100;0;0	2.39	False		ENSG00000101310	ENSG00000101310	HGNC:10702