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
CYP2C8	gene	CYP2C8	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	Unknown	Rhabdomyolysis, cerivastatin-induced;{Drug metabolism, altered, CYP2C8-related}, OMIM:618018				20739906;15365880		False	1	0;0;100	2.10	False		ENSG00000138115	ENSG00000138115	HGNC:2622													
PHKB	gene	PHKB	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	BIALLELIC, autosomal or pseudoautosomal	Phosphorylase kinase deficiency of liver and muscle, autosomal recessive, OMIM:261750						False	1	0;0;100	2.10	False		ENSG00000102893	ENSG00000102893	HGNC:8927													
PHKG1	gene	PHKG1	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	Unknown							False	1	0;0;100	2.10	False		ENSG00000164776	ENSG00000164776	HGNC:8930													
SLC22A12	gene	SLC22A12	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	BIALLELIC, autosomal or pseudoautosomal	Exercise induced acute kidney failure;Hypouricemia, renal, OMIM:220150						False	1	0;0;100	2.10	False		ENSG00000197891	ENSG00000197891	HGNC:17989													
SLC2A9	gene	SLC2A9	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Hypouricemia, renal, 2, OMIM:612076;Exercise induced kidney injury						False	1	0;0;100	2.10	False		ENSG00000109667	ENSG00000109667	HGNC:13446													
TSEN54	gene	TSEN54	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	BIALLELIC, autosomal or pseudoautosomal	Pontocerebellar hypoplasia type 2A, OMIM:277470				25929793;23177318		False	1	0;0;100	2.10	False		ENSG00000182173	ENSG00000182173	HGNC:27561													
TSFM	gene	TSFM	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 3, OMIM:610505				17033963		False	1	0;0;100	2.10	False		ENSG00000123297	ENSG00000123297	HGNC:12367													
TYMP	gene	TYMP	Expert Review Red;NHS GMS	Acute rhabdomyolysis		Neurology	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 1 (MNGIE type), OMIM:603041				24199812		False	1	0;0;100	2.10	False		ENSG00000025708	ENSG00000025708	HGNC:3148													
XPNPEP3	gene	XPNPEP3	Literature	Acute rhabdomyolysis		Neurology	BIALLELIC, autosomal or pseudoautosomal	myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis, MONDO:0859322				40953058		False	1	0;0;100	2.10	False		ENSG00000196236	ENSG00000196236	HGNC:28052