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
C8G	gene	C8G	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	Unknown				Abnormality of complement system;HP:0005339			False	1	0;0;100	1.2	True		ENSG00000176919	ENSG00000176919	HGNC:1354													
CFHR4	gene	CFHR4	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	Unknown				Abnormality of complement system;HP:0005339			False	1	0;0;100	1.2	True		ENSG00000134365	ENSG00000134365	HGNC:16979													
FCN3	gene	FCN3	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency due to ficolin 3 deficiency, MIM# 613860			Abnormality of complement system;HP:0005339	25662573;22226667;19535802;20971976		False	1	0;0;100	1.2	True		ENSG00000142748	ENSG00000142748	HGNC:3625													
ITGAM	gene	ITGAM	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	Unknown				Abnormality of complement system;HP:0005339			False	1	0;0;100	1.2	True		ENSG00000169896	ENSG00000169896	HGNC:6149													
MASP2	gene	MASP2	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	MASP2 deficiency, MIM# 613791			Abnormality of complement system;HP:0005339	31828694		False	1	0;0;100	1.2	True		ENSG00000009724	ENSG00000009724	HGNC:6902													
THBD	gene	THBD	Expert Review Green;Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Hemolytic uremic syndrome, atypical, susceptibility to, 6}, MIM# 612926			Abnormality of complement system;HP:0005339	29500241;19625716		False	1	0;0;100	1.2	True		ENSG00000178726	ENSG00000178726	HGNC:11784