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
GRB10	gene	GRB10	Expert Review Amber;Literature	Multi locus imprinting disorders		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)	Silver-Russell syndrome 2, OMIM:618905				10861285;10856193;27370225;10856193;11112662;30794780;http://igc.otago.ac.nz/home.html		False	2	100;0;0	1.18	False		ENSG00000106070	ENSG00000106070	HGNC:4564													
PLAGL1	gene	PLAGL1	Expert Review Amber;Literature	Multi locus imprinting disorders		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)	"{Diabetes mellitus, transient neonatal 1}	, OMIM:601410"				16928428;7719335;8842729;11935319;17084362;10655556;30794780;http://igc.otago.ac.nz/home.html		False	2	100;0;0	1.18	False		ENSG00000118495	ENSG00000118495	HGNC:9046													
ZFP57	gene	ZFP57	Expert list;Expert Review Amber	Multi locus imprinting disorders		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	{Diabetes mellitus, transient neonatal 1}, OMIM:601410;Multi-locus imprinting disturbance (MLID)				35296332;39090763		False	2	100;0;0	1.18	False		ENSG00000204644	ENSG00000204644	HGNC:18791