Atrial Fibrillation, Familial, 6; Atfb6

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

Atrial fibrillation (AF) is the most common sustained cardiac rhythm disturbance, affecting more than 2 million Americans, with an overall prevalence of 0.89%. The prevalence increases rapidly with age, to 2.3% between the ages of 40 and 60 years, and to 5.9% over the age of 65. The most dreaded complication is thromboembolic stroke (Brugada et al., 1997).For a discussion of genetic heterogeneity of atrial fibrillation, see {608583}.

Genes related to Atrial Fibrillation, Familial, 6; Atfb6

NPPA
NPPA-AS1

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Atrial Fibrillation, Familial, 6; Atfb6

Hypertension
Cardiomyopathy
Stroke
Vertigo
Tachycardia
Atrial fibrillation
Palpitations
Thromboembolic stroke
Sick sinus syndrome

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Atrial Fibrillation, Familial, 6; Atfb6 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Atrial Fibrillation Panel. By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States). SCN1B, SCN2B, SCN5A, SCN3B, GJA5, ABCC9, KCNA5, KCND3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, LMNA, NPPA, NUP155 Specificity 7 % Genes 50 %
NPPA. By Institute for Human Genetics University Clinic Freiburg (Germany). NPPA Specificity 100 % Genes 50 %
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis. By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands). RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TNNT2, TRDN, CACNA1C, CACNA1D, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, SLMAP, HCN4 , (...) View the complete list with 27 more genes Panel complete gene list RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TNNT2, TRDN, CACNA1C, CACNA1D, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, SLMAP, HCN4, RANGRF, TRPM4, SCN3B, GPD1L, DPP6, AKAP9, GJA5, ANK2, ABCC9, KCNA5, KCND3, KCNE1, KCNE5, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LAMP2, LMNA, ASPH, NPPA, PKP2, PLN, PRKAG2 Specificity 3 % Genes 50 %
Atrial fibrillation, familial 6 (sequence analysis of NPPA gene). By CGC Genetics (Portugal). NPPA Specificity 100 % Genes 50 %
Familial Atrial Fibrillation Syndrome Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SCN1B, SCN2B, SCN5A, SCN3B, GJA5, ABCC9, KCNA5, KCND3, KCNE1, KCNE5, KCNE2, KCNH2, KCNJ2, KCNQ1, NPPA Specificity 7 % Genes 50 %
Atrial Fibrillation Syndrome via NPPA Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). NPPA Specificity 100 % Genes 50 %
Comprehensive Cardiology Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). RYR1, RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SGCD, SGCG, BRAF, SLC25A4, SNTA1, SOS1, SREBF2, TAZ, TBX3, TBX5, TCAP, TGFB2, TGFB3 , (...) View the complete list with 143 more genes Panel complete gene list RYR1, RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SGCD, SGCG, BRAF, SLC25A4, SNTA1, SOS1, SREBF2, TAZ, TBX3, TBX5, TCAP, TGFB2, TGFB3, TGFBR2, KLF10, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN, TTR, VCL, ZIC3, ACTA1, ZBTB17, ACTA2, MYOZ2, SLC2A10, ABCG5, ABCG8, CACNA1C, CACNA2D1, PRDM16, CACNB2, LMF1, JPH2, ACTC1, CALM1, CRELD1, CASQ2, CAV3, CBL, SHOC2, CBS, LDB3, ANKRD1, SALL4, ZHX3, SELENON, TRIM63, MYLK2, ACTN2, HCN4, APOA5, RANGRF, TRPM4, FKRP, LDLRAP1, CETP, CREB3L3, CALR3, SCN3B, PDLIM3, MIB1, COL3A1, COL5A2, COX15, MYPN, DOLK, CRYAB, CSRP3, NKX2-5, GPIHBP1, RBM20, DES, TMEM43, GPD1L, DMD, NEXN, GATAD1, DPP6, HSPB8, DSC2, DSG2, DSP, DNAJC19, DTNA, EFEMP2, ELN, EMD, CAVIN4, EYA4, FBN1, FBN2, FKTN, FHL1, FHL2, AKAP9, GAA, GCKR, GJA5, ALMS1, GLA, HADHA, HFE, ANK2, HRAS, ABCC9, APOA4, ILK, APOC2, APOE, JAG1, JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, KRAS, LAMA2, LAMA4, LAMP2, LDLR, LMNA, LTBP2, SMAD3, SMAD4, MAP2K1, MAP2K2, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYLK, MYO6, NODAL, NOTCH1, NPPA, NRAS, PKP2, PLN, PRKAG2, PRKAR1A, BAG3, PTPN11, RAF1 Specificity 1 % Genes 50 %
Comprehensive Cardiac Arrhythmia Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TGFB3, TNNI3, TRDN, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, LDB3, SLMAP , (...) View the complete list with 35 more genes Panel complete gene list RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TGFB3, TNNI3, TRDN, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, LDB3, SLMAP, HCN4, RANGRF, TRPM4, TNNI3K, SCN3B, NKX2-5, DES, TMEM43, GPD1L, DSC2, DSG2, DSP, AKAP9, GJA5, ANK2, ABCC9, JUP, KCNA5, KCND3, KCNE1, KCNE5, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNK3, KCNQ1, MYH6, MYL4, NPPA, PKP2, PLN, PRKAG2 Specificity 2 % Genes 50 %

You can get up to 26 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD VON WILLEBRAND DISEASE, TYPE 3; VWD3 TRICHORHINOPHALANGEAL SYNDROME, TYPE I; TRPS1 SPINOCEREBELLAR ATAXIA 4; SCA4 PACHYONYCHIA CONGENITA 2; PC2 EPILEPSY, PROGRESSIVE MYOCLONIC, 8; EPM8