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
CBS	gene	CBS	Expert list;Expert Review Amber	Pneumothorax	Structural lung disorders	Respiratory disorders	BIALLELIC, autosomal or pseudoautosomal	Classic homocystinuria MONDO:0009352			Pneumothorax;HP:0002107	2333882;27229674;9427154;30681372		False	2	0;100;0	2.3	True		ENSG00000160200	ENSG00000160200	HGNC:1550													
PRDM10	gene	PRDM10	Expert Review Amber;Literature	Pneumothorax	Structural lung disorders	Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Birt-Hogg-Dube syndrome 2, MIM# 620459			Pneumothorax;HP:0002107	36440963;37331486;40028672		False	2	0;100;0	2.3	True		ENSG00000170325	ENSG00000170325	HGNC:13995