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
ENG	gene	ENG	Expert Review Red;Illumina TruGenome Clinical Sequencing Services	Multiple bowel polyps	GI tract	Tumour syndromes	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Juvenile Polyposis						False	1	0;0;0	1.11	True		ENSG00000106991	ENSG00000106991	HGNC:3349													
GREM1	gene	GREM1	Expert Review Red;Radboud University Medical Center, Nijmegen;UKGTN	Multiple bowel polyps	GI tract	Tumour syndromes		{Colorectal cancer, increased risk, association with}(Peters (2012) Hum Genet 131,217);Oligosyndactyly of the hands, Cenani-Linz-like (Dimitrov (2010) J Med Genet 47,569);Mixed polyposis syndrome (Jaeger (2012) Nat Genet 44,699);Polyposis Syndrome, Hereditary Mixed, 1;Hereditary Mixed Polyposis Syndrome				Nat Genet. 2012 May 6;44(6):699-703. doi: 10.1038/ng.2263.		False	1	100;0;0	1.11	True		ENSG00000166923	ENSG00000166923	HGNC:2001