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
MSH6	gene	MSH6	Expert list;Expert Review Red	Predominantly Antibody Deficiency		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Mismatch repair cancer syndrome 3 MIM#619097;constitutional mismatch repair deficiency;immunodeficiency			Decreased immunoglobulin level;HP:0041078	22250089;32048120;30013564		False	1	0;0;100	1.0	True		ENSG00000116062	ENSG00000116062	HGNC:7329													
NFKBID	gene	NFKBID	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Predominantly Antibody Deficiency		Immunological disorders	Unknown				Decreased immunoglobulin level;HP:0041078	26973645;25347393;22761313		False	1	0;0;100	1.0	True		ENSG00000167604	ENSG00000167604	HGNC:15671													
TNFSF12	gene	TNFSF12	Expert Review Red;Melbourne Genomics Health Alliance Immunology Flagship;Victorian Clinical Genetics Services	Predominantly Antibody Deficiency		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Recurrent infections, poor antibody responses, decreased immunoglobulins			Decreased immunoglobulin level;HP:0041078	23493554		False	1	0;50;50	1.0	True		ENSG00000239697	ENSG00000239697	HGNC:11927													
TNFSF13	gene	TNFSF13	Expert Review Red;Literature	Predominantly Antibody Deficiency		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Hypogammaglobulinaemia, MONDO:0015977, TNSF13-related			Decreased immunoglobulin level;HP:0041078	PMID: 32298700		False	1	0;0;100	1.0	True		ENSG00000161955	ENSG00000161955	HGNC:11928