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
FOXF1	gene	FOXF1	Expert Review Green;NHS GMS	Alveolar capillary dysplasia with misalignment of pulmonary veins		Respiratory	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Alveolar capillary dysplasia with misalignment of pulmonary veins, OMIM:265380;alveolar capillary dysplasia with misalignment of pulmonary veins, MONDO:0009934						False	3	0;0;0	1.8	False		ENSG00000103241	ENSG00000103241	HGNC:3809													
LINC01081	gene	LINC01081	Expert Review Amber;NHS GMS	Alveolar capillary dysplasia with misalignment of pulmonary veins		Respiratory	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Alveolar capillary dysplasia with misalignment of pulmonary veins				19500772;23034409;24842713;27071622		False	2	100;0;0	1.8	False		ENSG00000268754	ENSG00000268754	HGNC:49124													
LINC01082	gene	LINC01082	Expert Review Amber;NHS GMS	Alveolar capillary dysplasia with misalignment of pulmonary veins		Respiratory	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Alveolar capillary dysplasia with misalignment of pulmonary veins				19500772;23034409;24842713;27071622		False	2	100;0;0	1.8	False		ENSG00000269186	ENSG00000269186	HGNC:49125