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
LOXL3	gene	LOXL3	Expert list;Expert Review Amber	Stickler Syndrome		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Stickler syndrome			Myopia;HP:0000545; Retinal detachment;HP:0000541; Cleft palate;HP:0000175	30362103;25663169		False	2	0;100;0	1.9	True		ENSG00000115318	ENSG00000115318	HGNC:13869													
SLC29A3	gene	SLC29A3	Expert list;Expert Review Amber;Literature	Stickler Syndrome		Ophthalmological disorders	BIALLELIC, autosomal or pseudoautosomal	Histiocytosis-lymphadenopathy plus syndrome - MIM#602782			Myopia;HP:0000545; Retinal detachment;HP:0000541; Cleft palate;HP:0000175			False	2	50;50;0	1.9	True		ENSG00000198246	ENSG00000198246	HGNC:23096