NUP155 gene related symptoms and diseases
All the information presented here about the NUP155 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,ORPHANET,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NUP155 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Tachycardia | Very Common - Between 80% and 100% cases |
| Atrial flutter | Very Common - Between 80% and 100% cases |
| Atrial fibrillation | Very Common - Between 80% and 100% cases |
| Pain | Uncommon - Between 30% and 50% cases |
| Abnormal heart morphology | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with NUP155 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Cardiomyopathy
- AV nodal tachycardia
- Abnormal electrophysiology of sinoatrial node origin
- Permanent atrial fibrillation
- Thromboembolic stroke
- ST segment elevation
- Abnormal atrioventricular conduction
- Paroxysmal atrial fibrillation
And 12 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NUP155 gene
Here you will find a list of rare diseases related to the NUP155. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
FAMILIAL ATRIAL FIBRILLATION
Alternate names
FAMILIAL ATRIAL FIBRILLATION Is also known as atrial fibrillation, autosomal dominant
Description
Familial atrial fibrillation is a rare, genetically heterogenous cardiac disease characterized by erratic activation of the atria with an irregular ventricular response, in various members of a single family. It may be asymptomatic or associated with palpitations, dyspnea and light-headedness. Concomitant rhythm disorders and cardiomyopathies are frequently reported.
Most common symptoms of FAMILIAL ATRIAL FIBRILLATION
- Pain
- Respiratory distress
- Arrhythmia
- Stroke
- Dilated cardiomyopathy
More info about FAMILIAL ATRIAL FIBRILLATION
ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15
Description
Atrial fibrillation (AF) is a supraventricular tachyarrhythmia characterized by uncoordinated atrial activation with consequent deterioration of atrial mechanical function. It is the most common sustained cardiac rhythm disturbance, and its prevalence increases as the population ages. An estimated 70,000 strokes each year are caused by atrial fibrillation (summary by Oberti et al., 2004).For a discussion of genetic heterogeneity of atrial fibrillation, see {608583}.
Most common symptoms of ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15
- Cardiomyopathy
- Abnormal heart morphology
- Tachycardia
- Atrial fibrillation
- Supraventricular tachycardia
More info about ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15
SOURCES: OMIM
Search interest in NUP155
Potential gene panels for NUP155 gene
Atrial Fibrillation Panel Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Atrial Fibrillation Panel that also includes the following genes: SCN1B SCN2B SCN5A SCN3B GJA5 ABCC9 KCNA5 KCND3 KCNE1 KCNE2
More info about this panel United States.
Atrial Fibrillation NGS Panel Panel
United States.
By Fulgent Genetics Fulgent Genetics Atrial Fibrillation NGS Panel that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A HCN4 SCN3B GATA4 GATA6 GJA5
More info about this panel United States.
NUP155 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the NUP155 gene.
More info about this panel United States.
Atrial Fibrillation Panel Panel
Finland.
By Blueprint Genetics Atrial Fibrillation Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN5A TBX5 CACNB2 LDB3 HCN4 SCN3B GATA6
More info about this panel Finland.
Arrhythmia Panel Panel
Finland.
By Blueprint Genetics Arrhythmia Panel that also includes the following genes: RYR2 SCN10A SCN1B SCN5A TBX5 TGFB3 TNNI3 TNNT2 TRDN TTN
More info about this panel Finland.
Comprehensive Cardiology Panel Panel
Finland.
By Blueprint Genetics Comprehensive Cardiology Panel that also includes the following genes: RIT1 RRAS RYR2 SCN10A SCN1B SCN5A SCNN1B SCNN1G SCO2 SDHA
More info about this panel Finland.
Familial Atrial Fibrillation , Panel Massive Sequencing (NGS) 13 Genes Panel
Spain.
By Reference Laboratory Genetics Familial Atrial Fibrillation , Panel Massive Sequencing (NGS) 13 Genes that also includes the following genes: SCN1B SCN2B SCN4B SCN5A SCN3B GJA5 ABCC9 KCNA5 KCNE2 KCNJ2
More info about this panel Spain.
Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes Panel
Spain.
By Reference Laboratory Genetics Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes that also includes the following genes: RYR2 SCN1B SCN2B SCN4B SCN5A SGCD SLC25A3 SLC6A4 SNTA1 TAZ
More info about this panel Spain.
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