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
STX16	gene	STX16	Expert Review Amber;Literature;NHS GMS	Familial hypoparathyroidism		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Pseudohypoparathyroidism, type IB OMIM:603233;pseudohypoparathyroidism type 1B:MONDO:0011301				14561710;15579741;15800843;33320452;32337648;35119251		False	2	33;67;0	3.5	False		ENSG00000124222	ENSG00000124222	HGNC:11431