Atrial Standstill 2; Atrst2

Table of contents:

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

Description

Atrial standstill (AS) is a rare condition characterized by the absence of electrical and mechanical activity in the atria. On surface ECG, AS is distinguished by bradycardia, junctional (usually narrow complex) escape rhythm, and absence of the P wave. Nearly 50% of patients with AS experience syncope. AS can be persistent or transient, and diffuse or partial (summary by Fazelifar et al., 2005).

Genes related to Atrial Standstill 2; Atrst2

NPPA

View recommended genes panels

Clinical Features

Top most frequent phenotypes and symptoms related to Atrial Standstill 2; Atrst2

Cardiomyopathy
Congestive heart failure
Dyspnea
Scarring
Stroke
Tachycardia
Tetraplegia
Syncope
Palpitations
Bradycardia

And another 5 symptoms. If you need more information about this disease we can help you.

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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.

Alternative names

Atrial Standstill 2; Atrst2 Is also known as cardiomyopathy, atrial dilated, with atrial standstill, atrial dilation and standstill.

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 Standstill 2; Atrst2 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 100 %
NPPA. By Institute for Human Genetics University Clinic Freiburg (Germany). NPPA Specificity 100 % Genes 100 %
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 100 %
Atrial fibrillation, familial 6 (sequence analysis of NPPA gene). By CGC Genetics (Portugal). NPPA Specificity 100 % Genes 100 %
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 100 %
Atrial Fibrillation Syndrome via NPPA Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). NPPA Specificity 100 % Genes 100 %
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 100 %
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 100 %

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Sources and references

You can check the following sources for additional information.

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