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
ATP6V0A4	gene	ATP6V0A4	Expert Review Red;Literature	Calcium and Phosphate disorders		Renal and urinary tract disorders; Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	renal tubular acidosis, distal, 3, with or without sensorineural hearing loss MONDO:0011268			Abnormal blood calcium levels;HP:0004363; Abnormal blood phosphate levels;HP:0100529	35738466		False	1	0;0;100	1.24	True		ENSG00000105929	ENSG00000105929	HGNC:866													
SBDS	gene	SBDS	Expert Review Green;Expert Review Red;KidGen_CalcPhos v38.1.0;Victorian Clinical Genetics Services	Calcium and Phosphate disorders		Renal and urinary tract disorders; Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	Shwachman-Diamond syndrome, MIM# 260400			Abnormal blood calcium levels;HP:0004363; Abnormal blood phosphate levels;HP:0100529			False	1	50;0;50	1.24	True		ENSG00000126524	ENSG00000126524	HGNC:19440													
SGK3	gene	SGK3	Expert Review Red;Literature	Calcium and Phosphate disorders		Renal and urinary tract disorders; Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypophosphatemic rickets			Abnormal blood calcium levels;HP:0004363; Abnormal blood phosphate levels;HP:0100529	31821448;21451460		False	1	0;0;100	1.24	True		ENSG00000104205	ENSG00000104205	HGNC:10812													
SLC9A3R1	gene	SLC9A3R1	Expert Review Red;KidGen_CalcPhos v38.1.0	Calcium and Phosphate disorders		Renal and urinary tract disorders; Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Nephrolithiasis/osteoporosis, hypophosphatemic, 2, MIM# 612287			Abnormal blood calcium levels;HP:0004363; Abnormal blood phosphate levels;HP:0100529	18784102		False	1	0;0;100	1.24	True		ENSG00000109062	ENSG00000109062	HGNC:11075