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
XIAP	gene	XIAP	Expert Review Green;NHS GMS	Haemophagocytic syndrome with absent XIAP expression		Immunology	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Lymphoproliferative syndrome, X-linked, 2, OMIM:300635;X-linked lymphoproliferative disease due to XIAP deficiency, MONDO:0010385						False	3	100;0;0	1.4	False		ENSG00000101966	ENSG00000101966	HGNC:592