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
C14orf80	gene	C14orf80	Expert Review Red;Literature	Adrenal insufficiency	Adrenal disorders	Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	Syndromic disease, MONDO:0002254			Adrenal insufficiency;HP:0000846; Congenital adrenal hypoplasia;HP:0008244	39979680;38252227;30842647		False	1	0;0;100	0.76	True		ENSG00000185347	ENSG00000185347	HGNC:20127													
GFER	gene	GFER	Expert Review Red;Literature	Adrenal insufficiency	Adrenal disorders	Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial disease, MONDO:0044970			Adrenal insufficiency;HP:0000846; Congenital adrenal hypoplasia;HP:0008244	26018198		False	1	0;0;100	0.76	True		ENSG00000127554	ENSG00000127554	HGNC:4236													
GPR161	gene	GPR161	Expert Review Red;Genomics England PanelApp	Adrenal insufficiency	Adrenal disorders	Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	Pituitary stalk interruption syndrome MONDO:0019828, GPR161-related			Adrenal insufficiency;HP:0000846; Congenital adrenal hypoplasia;HP:0008244	25322266		False	1	0;0;100	0.76	True		ENSG00000143147	ENSG00000143147	HGNC:23694													
SIX3	gene	SIX3	Expert Review Red;Genomics England PanelApp	Adrenal insufficiency	Adrenal disorders	Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Holoprosencephaly 2 (157170);Non-acquired combined pituitary hormone deficiency MONDO:0018762			Adrenal insufficiency;HP:0000846; Congenital adrenal hypoplasia;HP:0008244	35951005		False	1	0;0;100	0.76	True		ENSG00000138083	ENSG00000138083	HGNC:10889