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
FECH	gene	FECH	Expert Review Amber;Genomics England PanelApp;NHS Genomic Medicine Service	Metal Metabolism Disorders		Metabolic disorders	BIALLELIC, autosomal or pseudoautosomal	EPP1;177000 PROTOPORPHYRIA, ERYTHROPOIETIC, 1			Abnormality of iron homeostasis;HP:0011031;Abnormal blood transition element cation concentration;HP:0011030	20857522;26387792;28614581		False	2	0;0;0	0.45	False		ENSG00000066926	ENSG00000066926	HGNC:3647													
FXYD2	gene	FXYD2	Expert Review Amber	Metal Metabolism Disorders		Metabolic disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Renal hypomagnesemia 2 MONDO:0007937, Disorders of magnesium metabolism			Abnormality of iron homeostasis;HP:0011031;Abnormal blood transition element cation concentration;HP:0011030	17980699, 12763862, 18448590, 11062458, 25765846, 27014088		False	2	0;0;0	0.45	False		ENSG00000137731	ENSG00000137731	HGNC:4026													
TFRC	gene	TFRC	Expert Review Amber	Metal Metabolism Disorders		Metabolic disorders	BIALLELIC, autosomal or pseudoautosomal	Disorders of iron metabolism;TFRC-related combined immunodeficiency MONDO:0014760			Abnormality of iron homeostasis;HP:0011031;Abnormal blood transition element cation concentration;HP:0011030	26642240		False	2	0;0;0	0.45	False		ENSG00000072274	ENSG00000072274	HGNC:11763