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
EBP	gene	EBP	Expert Review;Expert Review Amber	Peroxisomal Disorders		Metabolic disorders	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Chondrodysplasia punctata, X-linked dominant (MIM#302960)			Peroxisomal disease;MONDO:0019053	12509714		False	2	0;100;0	0.54	True		ENSG00000147155	ENSG00000147155	HGNC:3133													
SCP2	gene	SCP2	Expert Review Amber;Victorian Clinical Genetics Services	Peroxisomal Disorders		Metabolic disorders	BIALLELIC, autosomal or pseudoautosomal	Leukoencephalopathy with dystonia and motor neuropathy, MIM#613724			Peroxisomal disease;MONDO:0019053	16685654;26497993		False	2	0;50;50	0.54	True		ENSG00000116171	ENSG00000116171	HGNC:10606