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
ADAR	gene	ADAR	Expert Review Red;Victorian Clinical Genetics Services	Photosensitivity Syndromes		Dysmorphic and congenital abnormality syndromes	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Dyschromatosis symmetrica hereditaria , MIM#127400			Cutaneous photosensitivity;HP:0000992			False	1	0;0;100	1.11	True		ENSG00000160710	ENSG00000160710	HGNC:225													
GTF2H4	gene	GTF2H4	Expert Review Red;Literature	Photosensitivity Syndromes		Dysmorphic and congenital abnormality syndromes	BIALLELIC, autosomal or pseudoautosomal	Xeroderma pigmentosum, complementation group J, MIM# 621435			Cutaneous photosensitivity;HP:0000992	40924495;40924475		False	1	0;0;100	1.11	True		ENSG00000213780	ENSG00000213780	HGNC:4658													
TYR	gene	TYR	Expert Review Red;Victorian Clinical Genetics Services	Photosensitivity Syndromes		Dysmorphic and congenital abnormality syndromes	Unknown	Albinism, oculocutaneous, type IA, MIM# 203100			Cutaneous photosensitivity;HP:0000992			False	1	0;0;100	1.11	True		ENSG00000077498	ENSG00000077498	HGNC:12442