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
PHF6	gene	PHF6	Expert Review Red;Victorian Clinical Genetics Services	Overgrowth		Dysmorphic and congenital abnormality syndromes	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Borjeson-Forssman-Lehmann syndrome, MIM# 301900			Overgrowth;HP:0001548; Tall stature;HP:0000098; Increased body weight;HP:0004324			False	1	0;0;100	1.14	True		ENSG00000156531	ENSG00000156531	HGNC:18145													
PTCH1	gene	PTCH1	Expert Review Red;Victorian Clinical Genetics Services	Overgrowth		Dysmorphic and congenital abnormality syndromes	Unknown	Basal cell nevus syndrome, MIM# 109400			Overgrowth;HP:0001548; Tall stature;HP:0000098; Increased body weight;HP:0004324			False	1	0;0;100	1.14	True		ENSG00000185920	ENSG00000185920	HGNC:9585													
RNF135	gene	RNF135	Expert Review Red;Victorian Clinical Genetics Services	Overgrowth		Dysmorphic and congenital abnormality syndromes	Unknown				Overgrowth;HP:0001548; Tall stature;HP:0000098; Increased body weight;HP:0004324			False	1	0;0;100	1.14	True		ENSG00000181481	ENSG00000181481	HGNC:21158