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
EPAS1	gene	EPAS1	Expert list;Expert Review Amber	Inherited phaeochromocytoma and paraganglioma excluding NF1		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Erythrocytosis, familial, 4, OMIM:611783				22931260;23418310;33300499		False	2	0;100;0	4.2	False		ENSG00000116016	ENSG00000116016	HGNC:3374													
PRKAR1A	gene	PRKAR1A	Expert Review Amber;NHS GMS	Inherited phaeochromocytoma and paraganglioma excluding NF1		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Endocrine Cancer;Carney complex						False	2	0;100;0	4.2	True		ENSG00000108946	ENSG00000108946	HGNC:9388