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
RAB5B	gene	RAB5B	Expert Review Amber;NHS GMS	Childhood interstitial lung disease		Respiratory	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	interstitial lung disease, MONDO:0015925				35121658		False	2	0;100;0	1.6	False		ENSG00000111540	ENSG00000111540	HGNC:9784													
TMEM63B	gene	TMEM63B	Expert Review Amber;Literature	Childhood interstitial lung disease		Respiratory	BIALLELIC, autosomal or pseudoautosomal	autosomal-recessive TMEM63B-related syndromic surfactant dysfunction disorder;lung disorder, MONDO:0005275				42259295		False	2	100;0;0	1.6	False		ENSG00000137216	ENSG00000137216	HGNC:17735