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
CASR	gene	CASR	Expert Review Green;NHS GMS	Calcium-sensing receptor phenotypes		Endocrinology	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Hypocalciuric hypercalcemia, type I, OMIM:145980;Hyperparathyroidism, neonatal, OMIM:239200;Hypocalcemia, autosomal dominant, OMIM:601198;Hypocalcemia, autosomal dominant, with Bartter syndrome, OMIM:601198;familial hypocalciuric hypercalcemia 1, MONDO:0007791;neonatal severe primary hyperparathyroidism,  MONDO:0009397;autosomal dominant hypocalcemia 1, MONDO:0011013						False	3	100;0;0	1.3	False		ENSG00000036828	ENSG00000036828	HGNC:1514