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 Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Oligodontia-colorectal cancer syndrome, MIM# 608615				15042511;21626677;21416598		False	3	100;0;0	0.29	True		ENSG00000168646	ENSG00000168646	HGNC:904													
EDA	gene	EDA	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ectodermal dysplasia 1, hypohidrotic, X-linked MIM#305100;Tooth agenesis, selective, X-linked 1 MIM#313500				27144394;8696334;9507389;9683615;18657636		False	3	100;0;0	0.29	True		ENSG00000158813	ENSG00000158813	HGNC:3157													
EDAR	gene	EDAR	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884;autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619				10431241;20301291;16435307;20979233;23401279;18384562		False	3	100;0;0	0.29	True		ENSG00000135960	ENSG00000135960	HGNC:2895													
EDARADD	gene	EDARADD	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	autosomal dominant hypohidrotic ectodermal dysplasia MONDO:0015884;autosomal recessive hypohidrotic ectodermal dysplasia MONDO:0016619				20301291;34219261;11780064;26991760;34573371;20979233;17354266;26440664		False	3	100;0;0	0.29	True		ENSG00000186197	ENSG00000186197	HGNC:14341													
IKBKG	gene	IKBKG	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Ectodermal dysplasia and immunodeficiency 1, MIM# 300291;Immunodeficiency 33 , MIM#300636;Incontinentia pigmenti, MIM# 308300						False	3	100;0;0	0.29	True		ENSG00000073009	ENSG00000269335	HGNC:5961													
KRT17	gene	KRT17	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	Unknown							False	3	100;0;0	0.29	False		ENSG00000128422	ENSG00000128422	HGNC:6427													
LRP6	gene	LRP6	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	Unknown							False	3	0;0;0	0.29	False		ENSG00000070018	ENSG00000070018	HGNC:6698													
MSX1	gene	MSX1	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	Unknown							False	3	0;0;0	0.29	False		ENSG00000163132	ENSG00000163132	HGNC:7391													
PAX9	gene	PAX9	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Tooth agenesis, selective, 3 - MIM#604625				10615120;16479262		False	3	100;0;0	0.29	True		ENSG00000198807	ENSG00000198807	HGNC:8623													
SMOC2	gene	SMOC2	Expert Review Green;Literature;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Dentin dysplasia, type I, with microdontia and misshapen teeth, MIM# 125400				22152679;23317772;32908163		False	3	100;0;0	0.29	True		ENSG00000112562	ENSG00000112562	HGNC:20323													
WNT10A	gene	WNT10A	Expert Review Green;Victorian Clinical Genetics Services	Oligodontia		Dysmorphic and congenital abnormality syndromes	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Odontoonychodermal dysplasia 257980 AR;Schopf-Schulz-Passarge syndrome 224750 AR;Tooth agenesis, selective, 4 150400 AR, AD				19559398;30426266		False	3	100;0;0	0.29	True		ENSG00000135925	ENSG00000135925	HGNC:13829													
WNT10B	gene	WNT10B	Expert Review Green;Literature	Oligodontia		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	"Tooth agenesis, selective, 8	MIM#617073"				27321946;29364501;21554266;31050392		False	3	100;0;0	0.29	True		ENSG00000169884	ENSG00000169884	HGNC:12775