Painel geral de cardiomiopatias [227 genes]

Serviços > Cardiologia > Cardiopatias congénitas e hipertensão pulmonar > Painel geral de cardiomiopatias [227 genes]

Genes

GEN_NGS0006

ACTC1	SCN5A	COX15	GYG1	MYZAP	SPEG	CBL*	LDB3*	PKP4*	WISP1*
BAG3	TNNC1	COX6B1	GYS1	NAA10	SURF1	CDC25B*	LEMD2*	PPP1CB*	XK*
DES	TNNI3	CRYAB	HCN4	NDUFB11	TAZ	CDH2*	LMOD2*	PPP1R13L*
DMD	TNNT2	CSRP3	HFE	NF1	TBX5	CHRM2*	LRRC10*	PSEN1*
DSC2	TPM1	CTNNA3	HRAS	NRAS	TBX20	COL7A1*	MEF2C*	PSEN2*
DSG2	TRIM63	DLD	JPH2	PCCA	TCAP	CTF1*	MIB1*	RBM24*
DSP	TTN	DNAJC19	KCNJ2	PCCB	TMEM43	CTNNA1*	MYH6*	RRAS*
EMD	TTR	DOLK	KLHL24	PLEKHM2	TMEM70	CTNNB1*	MYLK2*	SGCA*
FHL1	AARS2	DTNA	KLF5	PMM2	TNNI3K	DNM1L*	MYLK3*	SGCB*
FHOD3	ACAD9	DYSF	KRAS	PPA2	VARS2	ELAC2*	MYOM1*	SLC25A4*
FLNC	ACADVL	EYA4	LAMA2	PPCS	ZBTB17	FBXO32*	NEBL*	SOS2*
GLA	ACTA1	FAH	LIAS	PRDM16	ABCC9*	FXN*	NEXN*	SPRED1*
JUP	ACTN2	FHL2	LZTR1	QRSL1	AKT1*	FOXD4*	NNT*	SYNE1*
LAMP2	AGK	FKRP	MAP2K1	RAF1	ANK2*	GATAD1*	NONO	SYNE2*
LMNA	AGL	FKTN	MAP2K2	RIT1	ANKRD1*	GSK3B*	NRAP*	TGFB3*
MYBPC3	AGPAT2	FNIP1	MLYCD	RPL3L	ATP5F1E*	HAND1*	NUBPL*	TJP1*
MYH7	ALMS1	FOXRED1	MRAS	RYR2	BRAF*	HAND2*	OBSCN	TLL2*
MYL2	ALPK3	GAA	MRPL3	SCO2	BSCL2*	IDH2*	P2RX7*	TMOD1*
MYL3	ANO5	GATA4	MRPL44	SDHA	C10orf71*	ILK*	PDHA1*	TOR1AIP1*
NKX2-5	ASNA1	GATA5	MRPS22	SGCD	CACNA1C*	ISL1*	PDLIM3*	TP63*
PKP2	ATPAF2	GATA6	MTO1	SGCG	CALR*	JARID2*	PDLIM5*	TRIM54*
PLN	CAV3	GFM1	MYBPHL	SHOC2	CALR3*	KAT2B*	PERP*	TSFM*
PRKAG2	COA5	GLB1	MYOT	SLC22A5	CASQ2*	KCNJ8*	PHKA1*	TUFM*
PTPN11	COA6	GNPTAB	MYOZ2	SLC25A3	CASZ1*	KLF10*	PHKB*	TXNRD2*
RBM20	COQ2	GUSB	MYPN	SOS1	CAVIN4*	LAMA4*	PKD2*	VCL*

Genes prioritários: Genes onde há evidências suficientes (clínicas e funcionais) a serem consideradas associadas à doença; estão incluídos nas diretrizes de prática clínica.
*Genes candidatos: Evidências insuficientes em humanos, mas potencialmente associadas à doença.