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
ALX3	gene	ALX3	Expert Review Amber;Victorian Clinical Genetics Services	Pierre Robin Sequence		Dysmorphic and congenital abnormality syndromes	Unknown				Pierre Robin sequence;HP:0000201			False	2	0;100;0	0.61	True		ENSG00000156150	ENSG00000156150	HGNC:449													
ALX4	gene	ALX4	Expert Review Amber;Victorian Clinical Genetics Services	Pierre Robin Sequence		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Frontonasal dysplasia 2, MIM# 613451;FND2 with alopecia			Pierre Robin sequence;HP:0000201	24668755;22140057;19692347		False	2	0;100;0	0.61	True		ENSG00000052850	ENSG00000052850	HGNC:450													
BMPR1B	gene	BMPR1B	Expert Review Amber;Literature	Pierre Robin Sequence		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	PRS;pectus excavatum;radioulnar synostosis			Pierre Robin sequence;HP:0000201	28418932		False	2	0;100;0	0.61	True		ENSG00000138696	ENSG00000138696	HGNC:1077													
EDN1	gene	EDN1	Expert Review Amber;Victorian Clinical Genetics Services	Pierre Robin Sequence		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Auriculocondylar syndrome 3, MIM# 615706			Pierre Robin sequence;HP:0000201	23315542;23913798;24268655		False	2	0;100;0	0.61	True		ENSG00000078401	ENSG00000078401	HGNC:3176