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
RMRP	gene	RMRP	Curated sources;Expert Review Red	Haematological malignancies for rare disease	Tumour syndromes	Tumour syndromes	BIALLELIC, autosomal or pseudoautosomal	Class: miscellaneous;Cartilage-hair hypoplasia syndrome;Non-hodgkin lymphoma Squamous carcinoma (bcc) Leukemia						False	1	100;0;0	1.19	False		ENSG00000269900	ENSG00000269900	HGNC:10031													
TERC	gene	TERC	Curated sources;Expert Review Red	Haematological malignancies for rare disease	Tumour syndromes	Tumour syndromes	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Class: BM failure syndrome (typ AR);Dyskeratosis congenita;MDS, AML;Bone marrow failure, macrocytosis;Skin, head and neck, and anogenital squamous cell cancers, Oral and GI squamous cell carcinoma				27881370; 28297620		False	1	100;0;0	1.19	False		ENSG00000270141	ENSG00000270141	HGNC:11727