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
ABCG2	gene	ABCG2	NHS GMS	Renal tubulopathies		Renal	Unknown	Serum uric acid concentration and susceptibility to gout, 138900						False	1	0;0;100	5.11	False		ENSG00000118777	ENSG00000118777	HGNC:74													
CLCNKA	gene	CLCNKA	Expert Review Red;NHS GMS	Renal tubulopathies		Renal	Other	Bartter syndrome, type 4b, digenic, OMIM:613090;Bartter disease type 4B, MONDO:0000909				15044642;18310267;32488762		False	1	0;100;0	5.11	False		ENSG00000186510	ENSG00000186510	HGNC:2026													
EGF	gene	EGF	NHS GMS	Renal tubulopathies		Renal		Hypomagnesemia 4, renal, 611718				17671655		False	1	0;0;100	5.11	False		ENSG00000138798	ENSG00000138798	HGNC:3229													
KCNA1	gene	KCNA1	NHS GMS	Renal tubulopathies		Renal		Autosomal dominant hypomagnesemia;Episodic ataxia/myokymia syndrome,160120				19307729		False	1	0;0;100	5.11	False		ENSG00000111262	ENSG00000111262	HGNC:6218													
SLC34A1	gene	SLC34A1	Expert Review Red;NHS GMS	Renal tubulopathies		Renal	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Hypercalcemia, infantile, 2, MIM 616963;Nephrolithiasis/osteoporosis, hypophosphatemic, 1, 612286;?Fanconi renotubular syndrome 2 613388				12324554;20335586		False	1	100;0;0	5.11	False		ENSG00000131183	ENSG00000131183	HGNC:11019													
SLC34A3	gene	SLC34A3	Expert Review Red;NHS GMS	Renal tubulopathies		Renal	BIALLELIC, autosomal or pseudoautosomal	Hypophosphatemic rickets with hypercalciuria, 241530				16358214;16358215;16849419		False	1	100;0;0	5.11	False		ENSG00000198569	ENSG00000198569	HGNC:20305													
SLC9A3R1	gene	SLC9A3R1	Expert Review Red;NHS GMS	Renal tubulopathies		Renal	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Nephrolithiasis/osteoporosis, hypophosphatemic, 2, 612287				18784102;25296721;19073985		False	1	100;0;0	5.11	False		ENSG00000109062	ENSG00000109062	HGNC:11075													
XPR1	gene	XPR1	Expert Review;Expert Review Red;Literature	Renal tubulopathies		Renal	Unknown	Fanconi syndrome;hypophosphatamia				27799484		False	1	0;0;100	5.11	False	Other	ENSG00000143324	ENSG00000143324	HGNC:12827