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
ALMS1	gene	ALMS1	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Alstrom syndrome, MIM#203800			Polydactyly;HP:0010442			False	1	0;0;100	0.281	True		ENSG00000116127	ENSG00000116127	HGNC:428													
ALX3	gene	ALX3	Expert Review Red;Genetic Health Queensland;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Frontonasal dysplasia 1, MIM#136760			Polydactyly;HP:0010442	19409524		False	1	0;0;100	0.281	True		ENSG00000156150	ENSG00000156150	HGNC:449													
ARMC8	gene	ARMC8	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	Unknown				Polydactyly;HP:0010442			False	1	0;0;100	0.281	True		ENSG00000114098	ENSG00000114098	HGNC:24999													
B9D1	gene	B9D1	Expert Review Red;Genetic Health Queensland;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Joubert syndrome 27, MIM#617120;Meckel syndrome 9, MIM#614209			Polydactyly;HP:0010442	24886560;21493627;25920555		False	1	0;0;100	0.281	True		ENSG00000108641	ENSG00000108641	HGNC:24123													
LRP4	gene	LRP4	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	"Cenani-Lenz syndactyly syndrome, MIM#	212780;Sclerosteosis 2, MIM#	614305"			Polydactyly;HP:0010442			False	1	0;0;100	0.281	True		ENSG00000134569	ENSG00000134569	HGNC:6696													
PNPLA6	gene	PNPLA6	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Laurence-Moon syndrome - MIM#245800;Boucher-Neuhauser syndrome - MIM#215470;Oliver-McFarlane syndrome - #275400;Spastic paraplegia 39, autosomal recessive - #612020			Polydactyly;HP:0010442	35069422;33818269;25299038;34157508;33210227;33141049;32758583;32586184;31135245;30097146;25574898		False	1	0;0;100	0.281	True		ENSG00000032444	ENSG00000032444	HGNC:16268													
PROM1	gene	PROM1	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Cone-rod dystrophy 12, MIM# 612657;Macular dystrophy, retinal, 2, MIM# 608051;Retinitis pigmentosa 41, MIM# 612095;Stargardt disease 4, MIM# 603786			Polydactyly;HP:0010442			False	1	0;0;100	0.281	True		ENSG00000007062	ENSG00000007062	HGNC:9454													
SDCCAG8	gene	SDCCAG8	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 16, MIM# 615993			Polydactyly;HP:0010442	20835237;22626039;22626039		False	1	0;0;100	0.281	True		ENSG00000054282	ENSG00000054282	HGNC:10671													
TBX22	gene	TBX22	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Cleft palate with ankyloglossia, MIM# 303400;Abruzzo-Erickson syndrome, MIM# 302905			Polydactyly;HP:0010442	11559848;12374769;14729838;17868388;22784330;22784330		False	1	0;0;100	0.281	True		ENSG00000122145	ENSG00000122145	HGNC:11600													
TRIM32	gene	TRIM32	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Bardet-Biedl syndrome 11, MIM# 615988			Polydactyly;HP:0010442	16606853		False	1	0;0;100	0.281	True		ENSG00000119401	ENSG00000119401	HGNC:16380													
ZNF141	gene	ZNF141	Expert Review Red;Victorian Clinical Genetics Services	Polydactyly		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Polydactyly, postaxial, type A6, MIM# 615226			Polydactyly;HP:0010442	23160277		False	1	0;0;100	0.281	True		ENSG00000131127	ENSG00000131127	HGNC:12926