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
CASP8	gene	CASP8	Expert Review Amber;Literature	Autoimmune Lymphoproliferative Syndrome		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Autoimmune lymphoproliferative syndrome, type IIB  MIM#607271				12353035;25814141;12654726;17213198;16148088		False	2	0;100;0	1.0	True		ENSG00000064012	ENSG00000064012	HGNC:1509													
RASGRP1	gene	RASGRP1	Expert Review Amber;Literature	Autoimmune Lymphoproliferative Syndrome		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	"Immunodeficiency 64	MIM#618534"				29155103;39752212		False	2	0;100;0	1.0	True		ENSG00000172575	ENSG00000172575	HGNC:9878													
