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
CEP19	gene	CEP19	Expert list;Expert Review Red	Bardet Biedl syndrome		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Bardet Biedl syndrome				29127258;24268657		False	1	0;0;100	1.10	True		ENSG00000174007	ENSG00000174007	HGNC:28209													
TRIM32	gene	TRIM32	Expert Review Red;Victorian Clinical Genetics Services	Bardet Biedl syndrome		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 11, MIM# 615988				16606853		False	1	0;0;100	1.10	True		ENSG00000119401	ENSG00000119401	HGNC:16380													
WDPCP	gene	WDPCP	Expert Review Red;Victorian Clinical Genetics Services	Bardet Biedl syndrome		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 15, MIM# 615992				20671153;25427950		False	1	0;0;100	1.10	True		ENSG00000143951	ENSG00000143951	HGNC:28027