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
MPZ	gene	MPZ	Expert Review Red;Literature	Auditory Neuropathy		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Syndromic auditory neuropathy spectrum disorder				21176974;12845552;12805115		False	1	0;0;100	1.1	True		ENSG00000158887	ENSG00000158887	HGNC:7225													
PCDH9	gene	PCDH9	Expert Review Red;Literature	Auditory Neuropathy		Neurology and neurodevelopmental disorders	Unknown	Non-syndromic auditory neuropathy spectrum disorder				21176974		False	1	0;0;100	1.1	True		ENSG00000184226	ENSG00000184226	HGNC:8661