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
WNT10A	gene	WNT10A	Expert Review Red;Victorian Clinical Genetics Services	Desmosomal disorders		Dermatological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Odontoonychodermal dysplasia 257980 AR Schopf-Schulz-Passarge syndrome 224750 AR Tooth agenesis, selective, 4 150400 AR, AD			Abnormal blistering of the skin;HP:0008066; Alopecia;HP:0001596	19559398;30426266		False	1	50;0;50	1.4	True		ENSG00000135925	ENSG00000135925	HGNC:13829