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
DACT1	gene	DACT1	Expert Review Red;NHS GMS	Radial Ray Abnormalities		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	?Townes-Brocks syndrome 2 (OMIM #617466)			Abnormality of radial ray;HP:0410049	PMID: 28054444;22610794;19701191		False	1	0;0;100	1.15	True		ENSG00000165617	ENSG00000165617	HGNC:17748													
FANCM	gene	FANCM	Expert Review Red;Victorian Clinical Genetics Services	Radial Ray Abnormalities		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Fanconi anaemia			Abnormality of radial ray;HP:0410049	28837162		False	1	0;0;100	1.15	True		ENSG00000187790	ENSG00000187790	HGNC:23168													
GATA1	gene	GATA1	Expert Review Red;Victorian Clinical Genetics Services	Radial Ray Abnormalities		Dysmorphic and congenital abnormality syndromes	Unknown				Abnormality of radial ray;HP:0410049			False	1	0;0;100	1.15	True		ENSG00000102145	ENSG00000102145	HGNC:4170													
RPS28	gene	RPS28	Expert Review Red;Victorian Clinical Genetics Services	Radial Ray Abnormalities		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Diamond Blackfan anemia 15 with mandibulofacial dysostosis, MIM# 606164			Abnormality of radial ray;HP:0410049	24942156		False	1	0;0;100	1.15	True		ENSG00000233927	ENSG00000233927	HGNC:10418