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
DDB1	gene	DDB1	Expert Review Red;UKGTN	Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome		Dermatology								False	1	0;0;100	3.7	False		ENSG00000167986	ENSG00000167986	HGNC:2717													
MARS	gene	MARS	Expert Review Red;Literature;NHS GMS	Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome		Dermatology	BIALLELIC, autosomal or pseudoautosomal	trichothiodystrophy, MONDO:0018053				33909043		False	1	33;0;67	3.7	False		ENSG00000166986	ENSG00000166986	HGNC:6898