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
DLST	gene	DLST	Expert list;Expert Review;Expert Review Red;Literature	Paraganglioma_phaeochromocytoma		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paragangliomas 7, MONDO:0032771;Pheochromocytoma, MONDO:0008233;Hereditary pheochromocytoma-paraganglioma, MONDO:0017366;Pheochromocytoma/paraganglioma syndrome 7, MIM#618475			Paraganglioma;HP:0002668; Phaeochromocytoma;HP:0002666	PMID: 30929736, 33180916		False	1	0;0;100	1.1	True		ENSG00000119689	ENSG00000119689	HGNC:2911													
EGLN1	gene	EGLN1	Expert list;Expert Review;Expert Review Red;Literature	Paraganglioma_phaeochromocytoma		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paraganglioma, MONDO:0000448;Pheochromocytoma, MONDO:0008233;Pheochromocytoma/paraganglioma, susceptibility to, no MIM#;Erythrocytosis, familial, 3, MIM#609820			Paraganglioma;HP:0002668; Phaeochromocytoma;HP:0002666	PMID: 19092153, 36013579		False	1	0;0;100	1.1	True		ENSG00000135766	ENSG00000135766	HGNC:1232													
EPAS1	gene	EPAS1	Expert list;Expert Review;Expert Review Red;Literature	Paraganglioma_phaeochromocytoma		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paraganglioma, MONDO:0000448;Pheochromocytoma, MONDO:0008233;Pheochromocytoma/paraganglioma, susceptibility to, no MIM#;Erythrocytosis, familial, 4, MIM#611783			Paraganglioma;HP:0002668; Phaeochromocytoma;HP:0002666	PMID: 22931260;23418310;33300499		False	1	0;0;100	1.1	True		ENSG00000116016	ENSG00000116016	HGNC:3374													
MDH2	gene	MDH2	Expert list;Expert Review;Expert Review Red;Literature	Paraganglioma_phaeochromocytoma		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paraganglioma, MONDO:0000448;Pheochromocytoma, MONDO:0008233;Pheochromocytoma/paraganglioma, susceptibility to, no MIM#;Developmental and epileptic encephalopathy 51, MIM#617339			Paraganglioma;HP:0002668; Phaeochromocytoma;HP:0002666	PMID: 25766404;30008476		False	1	0;0;100	1.1	True		ENSG00000146701	ENSG00000146701	HGNC:6971													
PRKAR1A	gene	PRKAR1A	Expert list;Expert Review;Expert Review Red;Literature	Paraganglioma_phaeochromocytoma		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paraganglioma, MONDO:0000448;Pheochromocytoma, MONDO:0008233;Carney complex, type 1, MIM#160980			Paraganglioma;HP:0002668; Phaeochromocytoma;HP:0002666			False	1	0;0;100	1.1	True		ENSG00000108946	ENSG00000108946	HGNC:9388													
SLC25A11	gene	SLC25A11	Expert list;Expert Review;Expert Review Red;Literature	Paraganglioma_phaeochromocytoma		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Paragangliomas 6, MONDO:0032767;Pheochromocytoma, MONDO:0008233;Hereditary pheochromocytoma-paraganglioma, MONDO:0017366;Pheochromocytoma/paraganglioma syndrome 6, MIM#618464			Paraganglioma;HP:0002668; Phaeochromocytoma;HP:0002666	PMID: 29431636		False	1	0;0;100	1.1	True		ENSG00000108528	ENSG00000108528	HGNC:10981