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
DBF4	gene	DBF4	Expert list;Expert Review Red	Phagocyte Defects		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	severe congenital neutropenia MONDO:0018542			Unusual infection;HP:0032101	36841265		False	1	0;0;100	1.33	True		ENSG00000006634	ENSG00000006634	HGNC:17364													
FPR1	gene	FPR1	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Phagocyte Defects		Immunological disorders	Unknown	Periodontitis			Unusual infection;HP:0032101	29105764;28371599		False	1	0;0;100	1.33	True		ENSG00000171051	ENSG00000171051	HGNC:3826