Painel geral de doenças cardiovasculares [406 genes]

Serviços > Cardiologia > Cardiopatias congénitas e hipertensão pulmonar > Painel geral de doenças cardiovasculares [406 genes]

Genes

GEN_NGS0008

ACTC1	TGFBR2	BMPR1B	ELAC2	KANSL1	NKX2-6	SLC22A8	ANK3*
ACVRL1	TMEM43	BSCL2	EP300	KCND2	NNT	SLC25A3	C10orf71*
APOB	TNNC1	CACNA1D	EVC	KCND3	NODAL	SLC25A4	CALR*
BAG3	TNNI3	CACNA2D1	EYA4	KCNE3	NOTCH2	SLC25A40	CASZ1*
BMPR2	TNNT2	CACNB2	FAH	KCNE5	NOTCH3	SLC2A10	CAVIN1*
BRAF	TPM1	CALM1	FBN2	KCNJ11	NPC1L1	SLC2A2	CDH2*
CACNA1C	TTN	CALM2	FHL1	KCNJ5	NPHP4	SLC39A13	CTNNA1*
CASQ2	TTR	CALM3	FHL2	KCNK17	NRAS	SLCO1B1	CTNNB1*
DES	A2ML1	CALR3	FHOD3	KLF11	OBSCN	SLMAP	DNM1L*
DMD	AARS2	CAV1	FKBP14	KMT2D	PAX4	SMAD1	FBXO32*
DSC2	ABCA1	CAV3	FKRP	LAMA2	PCDH15	SMAD3	FGF12*
DSG2	ABCB1	CAVIN4	FKTN	LAMA4	PCSK9	SMAD4	GREM2*
DSP	ABCC9	CBL	FLNA	LCAT	PDGFRA	SMAD6	GSK3B*
ELN	ABCG1	CBS	FOXC1	LDB3	PDHA1	SMAD9	IDH2*
EMD	ABCG5	CEL	FOXF1	LDLRAP1	PDX1	SNTA1	ILK*
ENG	ABCG8	CETP	FOXH1	LEFTY2	PHKA1	SPEG	IRX3*
FBN1	ACAD9	CFC1	FOXP1	LEP	PITX2	SPRED1	ISM2*
FLNC	ACADVL	CH25H	FOXP3	LIAS	PLIN1	SURF1	JARID2*
GATA4	ACTA1	CHD7	FOXRED1	LIPA	PLOD1	SYNE1	KAT6B*
GLA	ACTA2	CHRM2	FXN	LIPC	PLTP	SYNE2	KCNA5*
JAG1	ACTN2	CHST14	GAA	LMF1	PMM2	TAB2	KCNK3*
JUP	ACVR1	CIDEC	GATA5	LPA	PNPLA2	TBC1D4	KLF10*
KCNE1	ACVR2B	CITED2	GATA6	LPL	PPARA	TBX1	LMOD2*
KCNE2	ADAMTS2	COA5	GATAD1	LRP6	PPARG	TBX20	MAP3K8*
KCNH2	ADAMTSL4	COA6	GCK	LZTR1	PRDM16	TBX5	MEF2C*
KCNJ2	AGK	COL1A1	GDF1	MAP2K1	PRKG1	TCAP	MYLK2*
KCNJ8	AGL	COL1A2	GDF2	MAP2K2	PSEN1	TDGF1	NONO*
KCNQ1	AGPAT2	COL3A1	GFM1	MCTP2	PSEN2	TECRL	NOS1AP^*
KRAS	AKAP9	COL5A1	GJA1	MED12	PTF1A	TFAP2B	NOTCH1*
LAMP2	AKT1	COL5A2	GJA5	MED13L	PYGM	TGFB2	NPPA*
LDLR	AKT2	COL7A1	GLB1	MEF2A	RANGRF	TGFB3	NRAP*
LMNA	ALMS1	COQ2	GLIS3	MFAP5	RASA1	TGFBR1	OPA3*
LOX	AMPD1	COX15	GNPTAB	MIB1	RASA2	TMEM70	PDLIM3*
MYBPC3	ANGPTL3	COX6B1	GPD1	MLYCD	RFX6	TNNI3K	PERP*
MYH7	ANK2	CPT2	GPD1L	MRPL3	RIT1	TOPBP1	PKD2*
MYL2	ANKRD1	CREBBP	GPIHBP1	MRPL44	RRAS	TOR1AIP1	PKP4*
MYL3	ANO5	CRELD1	GUSB	MRPS22	RYR1	TRDN	PPP1CB*
NF1	APOA1	CRYAB	HAND2	MTO1	SALL4	TRIB1	PPP1R13L*
NKX2-5	APOA5	CSRP3	HCN4	MTTP	SAR1B	TRIM63	RBM24*
PKP2	APOC2	CTNNA3	HFE	MYH11	SCARB1	TRPM4	SGCA*
PLN	APOC3	CYP2D6	HNF1A	MYH6	SCN10A	TSFM	SGCB*
PRKAG2	APOE	CYP3A4	HNF1B	MYLIP	SCN2B	TXNRD2	SPRY1*
PTPN11	ASPH	CYP3A5	HNF4A	MYLK	SCN3B	UPF3B	SYNGAP1*
RAF1	ATP5F1E	DLD	HRAS	MYOM1	SCN4B	VCL	TMEM175*
RBM20	ATP7A	DNAJC19	IER3IP1	MYOT	SCO2	WFS1	TMOD1*
RYR2	ATPAF2	DOLK	INS	MYOZ2	SDHA	XK	TRIM54*
SCN1B	B3GAT3	DTNA	INSIG2	MYPN	SGCD	ZBTB17	WISP1*
SCN5A	B4GALT7	EFEMP2	INSR	NEBL	SGCG	ZDHHC9	WT1*
SOS1	BLK	EHMT1	IRX4	NEUROD1	SHOC2	ZFPM2	ZFHX3*
SOS2	BMP10	EIF2AK3	ISL1	NEUROG3	SKI	ZIC3
TAZ	BMPR1A	EIF2AK4	JPH2	NEXN	SLC22A5	ZMPSTE24

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.