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
BMP7	gene	BMP7	Expert Review Red;Literature	Craniosynostosis		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Non-syndromic metopic craniosynostosis				32266521		False	1	0;0;100	1.68	True	Other	ENSG00000101144	ENSG00000101144	HGNC:1074													
CHST3	gene	CHST3	Expert Review Red;Literature	Craniosynostosis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	143095 SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS				24300290		False	1	0;0;100	1.68	True		ENSG00000122863	ENSG00000122863	HGNC:1971													
FREM1	gene	FREM1	Expert Review Red;Victorian Clinical Genetics Services	Craniosynostosis		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Trigonocephaly 2, MIM# 614485				21931569		False	1	0;0;100	1.68	True		ENSG00000164946	ENSG00000164946	HGNC:23399													
GINS2	gene	GINS2	Expert Review Red;Literature	Craniosynostosis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Meier-Gorlin syndrome with craniosynostosis				34353863		False	1	0;0;100	1.68	True		ENSG00000131153	ENSG00000131153	HGNC:24575													
SCARF2	gene	SCARF2	Expert Review Red;Literature	Craniosynostosis		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Van den Ende-Gupta syndrome MIM#600920				23808541		False	1	0;0;100	1.68	True		ENSG00000244486	ENSG00000244486	HGNC:19869