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
C4A	gene	C4A	Expert Review Amber;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	C4a deficiency MIM#614380;susceptibility systemic lupus erythematosus			Abnormality of complement system;HP:0005339	22387014;22737222;15998580;10529130;15294999;32048120		False	2	0;100;0	0.74	True		ENSG00000244731	ENSG00000244731	HGNC:1323													
C4B	gene	C4B	Expert Review Amber;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	susceptibility to autoimmune disease;C4B deficiency MIM#614379			Abnormality of complement system;HP:0005339	34764957;12626442;22387014;17503323;32048120		False	2	0;100;0	0.74	True		ENSG00000224389	ENSG00000224389	HGNC:1324													
C8A	gene	C8A	Expert Review Amber;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	C8 deficiency, type I MIM#613790			Abnormality of complement system;HP:0005339	9759902;32769119		False	2	0;100;0	0.74	True		ENSG00000157131	ENSG00000157131	HGNC:1352													
CFB	gene	CFB	Expert Review Amber;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Complement Deficiencies		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Complement factor B deficiency, MIM# 615561			Abnormality of complement system;HP:0005339	24152280		False	2	0;100;0	0.74	True		ENSG00000243649	ENSG00000243649	HGNC:1037													
FCN3	gene	FCN3	Expert Review Amber;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	2	0;100;0	0.74	True		ENSG00000142748	ENSG00000142748	HGNC:3625