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
PMVK	gene	PMVK	Expert Review Red;Other	Familial disseminated superficial actinic porokeratosis	Keratodermas	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Porokeratosis 1, multiple types, 175800; POROKERATOSIS OF MIBELLI				26202976;26816331 (correction for PMID:26202976);27052676		False	1	0;0;100	1.4	False		ENSG00000163344	ENSG00000163344	HGNC:9141													
SSH1	gene	SSH1	Expert Review Red;Other	Familial disseminated superficial actinic porokeratosis	Keratodermas	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	disseminated superficial actinic porokeratosis; DSAP				15459975		False	1	0;0;100	1.4	False		ENSG00000084112	ENSG00000084112	HGNC:30579