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
CSPP1	gene	CSPP1	Expert Review Red;Other	Mosaic skin disorders		Dermatological disorders	Unknown	Inflammatory linear verrucous epidermal naevus (ILVEN)			Abnormality of skin pigmentation;HP:0001000	https://doi.org/10.1016/S2096-6911(21)00044-3		False	1	0;0;100	1.12	True	Other	ENSG00000104218	ENSG00000104218	HGNC:26193													
GJA1	gene	GJA1	Expert Review Red;Other	Mosaic skin disorders		Dermatological disorders	Unknown	Inflammatory linear verrucous epidermal naevus (ILVEN)			Abnormality of skin pigmentation;HP:0001000	27890787		False	1	0;0;100	1.12	True	Other	ENSG00000152661	ENSG00000152661	HGNC:4274													
PTPN11	gene	PTPN11	Expert Review Red;Genomics England PanelApp;NHS GMS	Mosaic skin disorders		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Noonan syndrome;Noonan syndrome with lentigines (LEOPARD)			Abnormality of skin pigmentation;HP:0001000	Mosaic case series shortly to be published by Kinsler group		False	1	0;0;100	1.12	True		ENSG00000179295	ENSG00000179295	HGNC:9644