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
PTCH2	gene	PTCH2	Expert Review;Expert Review Red;Literature	Basal Cell Cancer		Cancer Predisposition	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Basal cell carcinoma, MONDO:0020804;Nevoid basal cell carcinoma syndrome, MONDO:0007187			Basal cell carcinoma;HP:0002671	PMID: 34170463, 18285427, 23479190, 30820324, 38354379		False	1	0;0;100	1.1	True		ENSG00000117425	ENSG00000117425	HGNC:9586