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
FAM20B	gene	FAM20B	Expert Review Amber;Literature	Multiple joint dislocations and laxity	Skeletal dysplasias	Skeletal disorders	BIALLELIC, autosomal or pseudoautosomal	FAM20B GLYCOSAMINOGLYCAN XYLOSYLKINASE 611063	617662		Joint dislocation;HP:0001373; Joint laxity;HP:0001388	30847897		False	2	0;0;0	0.9	False		ENSG00000116199	ENSG00000116199	HGNC:23017