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
CCDC141	gene	CCDC141	Expert Review Amber;Literature	Hypogonadotropic hypogonadism	Hypothalamic and pituitary disorders	Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Normosmic IHH (no OMIM)				28324054;27014940		False	2	0;100;0	1.42	False		ENSG00000163492	ENSG00000163492	HGNC:26821													
CLPP	gene	CLPP	Expert list;Expert Review Amber	Hypogonadotropic hypogonadism	Hypothalamic and pituitary disorders	Endocrine disorders	BIALLELIC, autosomal or pseudoautosomal	Perrault syndrome 3, OMIM:614129				27899912;23541340;25956234;26970254;27087618;27650058		False	2	100;0;0	1.42	False		ENSG00000125656	ENSG00000125656	HGNC:2084													
SPRY4	gene	SPRY4	Expert list;Expert Review Amber;Literature;Radboud University Medical Center, Nijmegen	Hypogonadotropic hypogonadism	Hypothalamic and pituitary disorders	Endocrine disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hypogonadotropic hypogonadism 17 with or without anosmia, OMIM:615266				23643382;32389901		False	2	100;0;0	1.42	False		ENSG00000187678	ENSG00000187678	HGNC:15533