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
AARS	gene	AARS	Expert Review Amber;Literature;NHS GMS	Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome		Dermatology	BIALLELIC, autosomal or pseudoautosomal	trichothiodystrophy, MONDO:0018053				33909043		False	2	33;67;0	3.7	False		ENSG00000090861	ENSG00000090861	HGNC:20													
MRE11	gene	MRE11	Expert Review Amber;Literature	Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome		Dermatology	BIALLELIC, autosomal or pseudoautosomal	Nijmegen breakage syndrome-like severe microcephaly				21227757		False	2	0;100;0	3.7	False		ENSG00000020922	ENSG00000020922	HGNC:7230													
TARS	gene	TARS	Expert list;Expert Review Amber;NHS GMS	Xeroderma pigmentosum, Trichothiodystrophy or Cockayne syndrome		Dermatology	BIALLELIC, autosomal or pseudoautosomal	Trichothiodystrophy 7, nonphotosensitive, OMIM:618546				31374204		False	2	67;33;0	3.7	False		ENSG00000113407	ENSG00000113407	HGNC:11572