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
F3	gene	F3	Expert Review Amber;London South GLH;NHS GMS;Wessex and West Midlands GLH	Thrombophilia with a likely monogenic cause		Haematology	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Tissue factor deficiency (Factor III)						False	2	0;67;33	2.10	False		ENSG00000117525	ENSG00000117525	HGNC:3541													
PLAT	gene	PLAT	Expert Review Amber;London South GLH;NHS GMS;North West GLH;Wessex and West Midlands GLH;Yorkshire and North East GLH	Thrombophilia with a likely monogenic cause		Haematology	BIALLELIC, autosomal or pseudoautosomal	Thrombophilia, familial, due to decreased release of PLAT, OMIM:612348						False	2	40;40;20	2.10	False		ENSG00000104368	ENSG00000104368	HGNC:9051													
PLG	gene	PLG	Expert Review Amber;London South GLH;NHS GMS;North West GLH;Wessex and West Midlands GLH;Yorkshire and North East GLH	Thrombophilia with a likely monogenic cause		Haematology	BIALLELIC, autosomal or pseudoautosomal	Plasminogen deficiency, type I, OMIM:217090;Dysplasminogenemia, OMIM:217090				9684804;12850227;16849641;27976734;35244080		False	2	57;43;0	2.10	False		ENSG00000122194	ENSG00000122194	HGNC:9071													
PROCR	gene	PROCR	Expert Review Amber;London South GLH;NHS GMS;North West GLH;Wessex and West Midlands GLH;Yorkshire and North East GLH	Thrombophilia with a likely monogenic cause		Haematology	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	?Thrombophilia				24051141		False	2	0;80;20	2.10	False		ENSG00000101000	ENSG00000101000	HGNC:9452													
PROZ	gene	PROZ	Expert Review Amber;London South GLH;NHS GMS;Wessex and West Midlands GLH	Thrombophilia with a likely monogenic cause		Haematology	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Protein Z deficiency, OMIM:614024						False	2	0;67;33	2.10	False		ENSG00000126231	ENSG00000126231	HGNC:9460													
TFPI	gene	TFPI	Expert Review Amber;London South GLH;NHS GMS;Wessex and West Midlands GLH	Thrombophilia with a likely monogenic cause		Haematology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown							False	2	0;67;33	2.10	False		ENSG00000003436	ENSG00000003436	HGNC:11760