Genomics England

Congenital muscular dystrophy and congenital myopathy (Version: )

Relevant disorders: R432

Signed off date: 14 May 2024

Panel types: GMS Rare Disease, Component Of Super Panel, GMS signed-off

116 green entities

Entity rating	Entity	Mode of inheritance	Mode of pathogenicity	Tags
Green	ACTA1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	ACTN2	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	ADSSL1	BIALLELIC, autosomal or pseudoautosomal	Other	new-gene-name
Green	AR_CAG STR	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	N/A	STR
Green	ASCC1	BIALLELIC, autosomal or pseudoautosomal	Other	N/A
Green	ASCC3	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	B3GALNT2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	B4GAT1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	BET1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	BIN1	BIALLELIC, autosomal or pseudoautosomal	N/A	watchlist_moi
Green	CACNA1S	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	CAVIN1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	CFL2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	CHKB	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	COL12A1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	COL13A1	BIALLELIC, autosomal or pseudoautosomal	Other	treatable
Green	COL25A1	BIALLELIC, autosomal or pseudoautosomal	Other	N/A
Green	COL6A1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	COL6A2	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	COL6A3	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	COX6A2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	DAG1	BIALLELIC, autosomal or pseudoautosomal	N/A	watchlist_moi
Green	DMD	X-LINKED: hemizygous mutation in males, biallelic mutations in females	N/A	Skewed X-inactivation, gene-therapy-trial
Green	DMPK_CTG STR	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	N/A	STR
Green	DNAJB4	BIALLELIC, autosomal or pseudoautosomal	Other	N/A
Green	DNM2	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	watchlist_moi, missense
Green	DOK7	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	DOLK	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	DPM2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	DPM3	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	DTNA	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Other	N/A
Green	ECEL1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	EMD	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	N/A	N/A
Green	EPG5	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	FHL1	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	N/A	N/A
Green	FKBP14	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	FKRP	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	FKTN	BIALLELIC, autosomal or pseudoautosomal	N/A	structural-variant
Green	FXR1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	GBE1	BIALLELIC, autosomal or pseudoautosomal	Other	N/A
Green	GFER	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	GGPS1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	GMPPB	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	GOLGA2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	GOSR2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	HACD1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	HNRNPA2B1	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	N/A	N/A
Green	INPP5K	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	ISCA-37408-Loss 2p15p16.1 region (includes BCL11A) Loss region	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	ISCA-37420-Loss 17q21.3 recurrent region (includes KANSL1) Loss region	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	ISCA-37429-Loss 4p16.3 terminal (Wolf-Hirshhorn syndrome) region Loss region	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	ISPD	BIALLELIC, autosomal or pseudoautosomal	N/A	new-gene-name
Green	ITGA7	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	JAG2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	KBTBD13	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	missense
Green	KLHL40	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	KLHL41	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	KY	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	LAMA2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	LARGE1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	LETM1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	LMNA	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	LMOD3	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MAP3K20	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MEGF10	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MICU1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MLIP	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MSTO1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	Q2_24_MOI
Green	MTM1	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	N/A	N/A
Green	MYBPC1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	MYH2	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	MYH3	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	MYH7	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	MYL1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MYL2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MYMK	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MYO18B	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MYOD1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	MYPN	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	NEB	BIALLELIC, autosomal or pseudoautosomal	N/A	watchlist_moi
Green	ORAI1	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	missense
Green	PAX7	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	PIEZO2	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	PLEC	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	POGLUT1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	POMGNT1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	POMGNT2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	POMK	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	POMT1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	POMT2	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	PYROXD1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	RYR1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	treatable, pharmacogenetics
Green	RYR3	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	SCN4A	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	SELENON	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	SIL1	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	SLC25A4	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	SPEG	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	SPTBN4	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	STAC3	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	STIM1	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	missense
Green	SYNE1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	TMEM5	BIALLELIC, autosomal or pseudoautosomal	N/A	new-gene-name
Green	TNNC2	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	TNNI2	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	TNNT1	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	TNNT3	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	N/A	N/A
Green	TPM2	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	TPM3	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	N/A	N/A
Green	TRAPPC11	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	TRDN	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	TRIP4	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	TTN	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	UNC45B	BIALLELIC, autosomal or pseudoautosomal	N/A	N/A
Green	VMA21	X-LINKED: hemizygous mutation in males, biallelic mutations in females	N/A	N/A
Green	ZC4H2	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	N/A	N/A

Congenital muscular dystrophy and congenital myopathy (Version: 1.0)

Congenital muscular dystrophy and congenital myopathy (Version: )