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
ERCC3	gene	ERCC3	Expert Review Red;Literature	Ichthyosis		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Trichothiodystrophy 2, photosensitive MIM#616390			Ichthyosis;HP:0008064	9012405;28913623		False	1	0;0;100	1.11	True		ENSG00000163161	ENSG00000163161	HGNC:3435													
GJB3	gene	GJB3	Expert Review Red;Victorian Clinical Genetics Services	Ichthyosis		Dermatological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Erythrokeratodermia variabilis et progressiva 1 MIM#133200			Ichthyosis;HP:0008064			False	1	0;0;100	1.11	True		ENSG00000188910	ENSG00000188910	HGNC:4285													
GJB4	gene	GJB4	Expert Review Red;Victorian Clinical Genetics Services	Ichthyosis		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Erythrokeratodermia variabilis et progressiva 2 MIM#617524			Ichthyosis;HP:0008064			False	1	0;0;100	1.11	True		ENSG00000189433	ENSG00000189433	HGNC:4286													
LIPN	gene	LIPN	Expert Review Red;Victorian Clinical Genetics Services	Ichthyosis		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Ichthyosis, congenital, autosomal recessive 8, MIM# 613943			Ichthyosis;HP:0008064	21439540		False	1	0;0;100	1.11	True		ENSG00000204020	ENSG00000204020	HGNC:23452													
PEX7	gene	PEX7	Expert list;Expert Review Red	Ichthyosis		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Peroxisome biogenesis disorder 9B MIM#614879			Ichthyosis;HP:0008064	12522768		False	1	0;0;100	1.11	True		ENSG00000112357	ENSG00000112357	HGNC:8860													
PHYH	gene	PHYH	Expert list;Expert Review Red	Ichthyosis		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Refsum disease MIM#266500			Ichthyosis;HP:0008064	25604618;9326940		False	1	0;0;100	1.11	True		ENSG00000107537	ENSG00000107537	HGNC:8940