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
SGK3	gene	SGK3	Expert Review Red;Literature	Hypophosphataemia or rickets		Endocrine disorders; Skeletal disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypophosphatemic rickets				31821448		False	1	0;0;100	0.53	True		ENSG00000104205	ENSG00000104205	HGNC:10812													
SLC9A3R1	gene	SLC9A3R1	Expert Review Red;KidGen_CalcPhos v38.1.0	Hypophosphataemia or rickets		Endocrine disorders; Skeletal disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Nephrolithiasis/osteoporosis, hypophosphatemic, 2, MIM# 612287				18784102		False	1	0;0;100	0.53	False		ENSG00000109062	ENSG00000109062	HGNC:11075