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
ARMC5	gene	ARMC5	Expert list;Expert Review Green	Primary pigmented nodular adrenocortical disease		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	ACTH-independent macronodular adrenal hyperplasia 2, OMIM:615954				24283224;24601692;24708098;24905064		False	3	100;0;0	1.11	False		ENSG00000140691	ENSG00000140691	HGNC:25781													
PDE11A	gene	PDE11A	Expert Review Green;NHS GMS	Primary pigmented nodular adrenocortical disease		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Pigmented nodular adrenocortical disease, primary, 2, OMIM:610475				16767104		False	3	100;0;0	1.11	False		ENSG00000128655	ENSG00000128655	HGNC:8773													
PDE8B	gene	PDE8B	Expert Review Green;NHS GMS	Primary pigmented nodular adrenocortical disease		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Pigmented nodular adrenocortical disease, primary, 3, OMIM:614190				18272904		False	3	100;0;0	1.11	False		ENSG00000113231	ENSG00000113231	HGNC:8794													
PRKAR1A	gene	PRKAR1A	Expert Review Green;NHS GMS	Primary pigmented nodular adrenocortical disease		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Pigmented nodular adrenocortical disease, primary, 1, OMIM:610489				12213893		False	3	100;0;0	1.11	False		ENSG00000108946	ENSG00000108946	HGNC:9388