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
ARHGAP42	gene	ARHGAP42	Expert Review Red;Literature	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	BIALLELIC, autosomal or pseudoautosomal	Interstitial lung disease;systemic hypertension;immunological abnormalities			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	34232960		False	1	0;0;100	0.84	True		ENSG00000165895	ENSG00000165895	HGNC:26545