Painel geral de cardiomiopatias, arritmias e morte súbita [288 genes]

Serviços > Cardiologia > Cardiopatias congénitas e hipertensão pulmonar > Painel geral de cardiomiopatias, arritmias e morte súbita [288 genes]

Genes

GEN_NGS0007

ACTC1	PLN	CAV3	GYG1	MYZAP	TAZ	COL7A1*	LMOD2*	PPP1CB*	TOR1AIP1*
BAG3	PRKAG2	COA5	GYS1	NAA10	TBX20	CTF1*	LRRC10*	PPP1R13L*	TRIM54*
CACNA1C	PTPN11	COA6	HCN4	NDUFB11	TBX5	CTNNA1*	MAP3K8*	PSEN1*	TSFM*
CALM1	RBM20	COQ2	HFE	NF1	TCAP	CTNNB1*	MEF2C*	PSEN2*	TUFM*
CALM2	RYR2	COX15	HRAS	NRAS	TECRL	DNM1L*	MIB1*	RANGRF*	TXNRD2*
CALM3	SCN5A	COX6B1	IRX3	PMM2	TMEM43	ELAC2*	MYH6*	RASA1*	VCL*
CASQ2	TNNC1	CRYAB	JPH2	PPA2	TMEM70	FBXO32*	MYLK2*	RASA2*	WISP1*
DES	TNNI3	CSRP3	KCND3	PCCA	TNNI3K	FGF12*	MYLK3*	RBM24*	XK*
DMD	TNNT2	CTNNA3	KCNE3	PCCB	TRDN	FOXD4*	MYOM1*	RNF207*	ZFHX3*
DSC2	TPM1	DLD	KCNE5	PLEKHM2	TRPM4	FXN*	NEBL*	RRAD*
DSG2	TRIM63	DNAJC19	KCNJ5	PPCS	VARS2	GATAD1*	NEXN*	RRAS*
DSP	TTN	DOLK	KCNJ8	PRDM16	ZBTB17	GJA1*	NKX2-6*	SCN10A*
EMD	TTR	DTNA	KLF5	QRSL1	A2ML1*	GPD1L*	NNT*	SCN3B*
FHL1	AARS2	DYSF	KLHL24	RAF1	ABCC9*	GREM2*	NONO*	SCN4B*
FHOD3	ACAD9	EYA4	KRAS	RIT1	AKT1*	GSK3B*	NOS1AP*	SEMA3A*
FLNC	ACADVL	FAH	LAMA2	RPL3L	ANKRD1*	HAND1*	NPPA*	SGCA*
GLA	ACTA1	FHL2	LIAS	SCN1B	ATP1A3*	HAND2*	NRAP*	SGCB*
JUP	ACTN2	FKRP	LZTR1	SCN2B	ATP5F1E*	IDH2*	NUBPL*	SHOX2*
KCNE1	AGK	FKTN	MAP2K1	SCN4A	BRAF*	ILK*	NUP155*	SLC25A4*
KCNE2	AGL	FNIP1	MAP2K2	SCO2	BSCL2*	ISL1*	OBSCN*	SLMAP*
KCNH2	AGPAT2	FOXRED1	MLYCD	SDHA	BVES*	JARID2*	P2RX7*	SOS2*
KCNJ2	AKAP9	GAA	MRAS	SGCD	C10orf71*	KAT2B*	PDHA1*	SPRED1*
KCNQ1	ALMS1	GATA4	MRPL3	SGCG	CALR*	KAT6B*	PDLIM3*	SPRY1*
LAMP2	ALPK3	GATA5	MRPL44	SHOC2	CALR3*	KCNA5*	PDLIM5*	SYNE1*
LMNA	ANK2	GATA6	MRPS22	SLC22A5	CASZ1*	KCND2*	PERP*	SYNE2*
MYBPC3	ANO5	GFM1	MTO1	SLC25A3	CAVIN1*	KCNJ3*	PHKA1*	SYNGAP1*
MYH7	ATPAF2	GJA5	MYBPHL	SLC4A3	CAVIN4*	KCNK17*	PHKB*	TGFB3*
MYL2	ASNA1	GLB1	MYL4	SNTA1	CBL*	KLF10*	PITX2*	TJP1*
MYL3	CACNA1D	GNB2	MYOT	SOS1	CDC25B*	LAMA4*	PKD2*	TLL2*
NKX2-5	CACNA2D1	GNPTAB	MYOZ2	SPEG	CDH2*	LEMD2*	PKP4*	TMOD1*
PKP2	CACNB2	GUSB	MYPN	SURF1	CHRM2*	LDB3*	POPDC2*	TP63*

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.