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
B3GNT4	gene	B3GNT4	Literature	Limb-Girdle Muscular Dystrophy and Distal Myopathy		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Hereditary neurological disease, MONDO:0100545, B3GNT4-related			Limb-girdle muscular dystrophy;MONDO:0016971; Proximal muscle weakness;HP:0003701; Distal myopathy MONDO:0018949	41444428		False	1	0;0;100	2.0	False		ENSG00000176383	ENSG00000176383	HGNC:15683													
TRIM72	gene	TRIM72	Expert Review Red;Literature	Limb-Girdle Muscular Dystrophy and Distal Myopathy		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Limb girdle muscular dystrophy MONDO:0016971, TRIM72-related			Limb-girdle muscular dystrophy;MONDO:0016971; Proximal muscle weakness;HP:0003701; Distal myopathy MONDO:0018949	40804694		False	1	0;0;100	2.0	True		ENSG00000177238	ENSG00000177238	HGNC:32671