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
KIF15	gene	KIF15	Expert Review Red;Literature	Pierre Robin Sequence		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Braddock-Carey syndrome 2 - MIM#619981			Pierre Robin sequence;HP:0000201	28150392		False	1	0;100;0	0.47	True		ENSG00000163808	ENSG00000163808	HGNC:17273													
TSR2	gene	TSR2	Expert Review Red;Victorian Clinical Genetics Services	Pierre Robin Sequence		Dysmorphic and congenital abnormality syndromes	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, MIM# 300946			Pierre Robin sequence;HP:0000201	24942156		False	1	0;0;100	0.47	True		ENSG00000158526	ENSG00000158526	HGNC:25455