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
CARD14	gene	CARD14	Other	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Pityriasis rubra pilaris, OMIM:173200;Thick scales on the scalp and areas of superficial peeling on the face, palms, soles, and genital region						False	1	0;0;100	1.5	False		ENSG00000141527	ENSG00000141527	HGNC:16446													
CHST8	gene	CHST8	Expert Review Red;Literature	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	?Peeling skin syndrome 3, 616265; OMIM:#616265;Peeling skin HP:0040189;Ichthyosis HP:0008064				PMID: 22289416		False	1	0;0;100	1.5	False		ENSG00000124302	ENSG00000124302	HGNC:15993													
EDA	gene	EDA	Other	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ectodermal dysplasia 1, hypohidrotic, X-linked, 305100; Skin peeling/scaling (newborn)						False	1	0;0;100	1.5	False		ENSG00000158813	ENSG00000158813	HGNC:3157													
KRT1	gene	KRT1	Other	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Epidermolytic hyperkeratosis, 113800; EHK; Islands of superficial peeling on the skin of the trunk and the extensor surface of the legs						False	1	0;0;100	1.5	False		ENSG00000167768	ENSG00000167768	HGNC:6412													
KRT10	gene	KRT10	Other	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Epidermolytic hyperkeratosis, 113800; EHK						False	1	0;0;100	1.5	False		ENSG00000186395	ENSG00000186395	HGNC:6413													
KRT2	gene	KRT2	Other	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Ichthyosis bullosa of Siemens, 146800; blistering, superficial peeling of the skin, and localized lichenified hyperkeratosis						False	1	0;0;100	1.5	False		ENSG00000172867	ENSG00000172867	HGNC:6439													
TP63	gene	TP63	Other	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Hay-Wells syndrome, 106260; Red, cracking, peeling skin at birth 						False	1	0;0;100	1.5	False		ENSG00000073282	ENSG00000073282	HGNC:15979													
TRPV3	gene	TRPV3	Other	Peeling skin syndrome	Skin fragility disorders	Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Olmsted syndrome, 614594; superficial peeling of the skin						False	1	0;0;100	1.5	False		ENSG00000167723	ENSG00000167723	HGNC:18084