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
SLC35F1	gene	SLC35F1	Expert Review Amber;Literature	Angelman Rett like syndromes		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder, MONDO:0700092, SLC35F1-associated;Rett-like syndrome				33821533		False	2	0;100;0	1.11	True		ENSG00000196376	ENSG00000196376	HGNC:21483													
UBTF	gene	UBTF	Expert Review Amber;Victorian Clinical Genetics Services	Angelman Rett like syndromes		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodegeneration, childhood-onset, with brain atrophy, MIM# 617672;MONDO:0044701				28777933;29300972		False	2	0;100;0	1.11	True		ENSG00000108312	ENSG00000108312	HGNC:12511