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
AXIN2	gene	AXIN2	Expert Review;Expert Review Amber	Ectodermal Dysplasia		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Oligodontia-colorectal cancer syndrome, MIM# 608615			Ectodermal dysplasia;HP:0000968	15042511;21626677;21416598;34637023		False	2	0;100;0	0.86	True		ENSG00000168646	ENSG00000168646	HGNC:904													
IFT43	gene	IFT43	Expert list;Expert Review Amber;Expert Review Green;Victorian Clinical Genetics Services	Ectodermal Dysplasia		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Cranioectodermal dysplasia 3 MIM#614099			Ectodermal dysplasia;HP:0000968	21378380;29896747		False	2	50;50;0	0.86	True		ENSG00000119650	ENSG00000119650	HGNC:29669													
KREMEN1	gene	KREMEN1	Expert list;Expert Review Amber;Royal Melbourne Hospital	Ectodermal Dysplasia		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Ectodermal dysplasia 13, hair/tooth type, 617392			Ectodermal dysplasia;HP:0000968	29526031;29526031		False	2	0;100;0	0.86	True		ENSG00000183762	ENSG00000183762	HGNC:17550													
TUFT1	gene	TUFT1	Expert Review;Expert Review Amber	Ectodermal Dysplasia		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Woolly hair-skin fragility syndrome, MIM# 620415			Ectodermal dysplasia;HP:0000968	36689522		False	2	0;100;0	0.86	True		ENSG00000143367	ENSG00000143367	HGNC:12422