Amyotrophic Lateral Sclerosis 15 With Or Without Frontotemporal Dementia; Als15
Genes related to Amyotrophic Lateral Sclerosis 15 With Or Without Frontotemporal Dementia; Als15
- UBQLN2
Clinical Features
Top most frequent phenotypes and symptoms related to Amyotrophic Lateral Sclerosis 15 With Or Without Frontotemporal Dementia; Als15
- Dysarthria
- Dysphagia
- Dystonia
- Dementia
- Pallor
- Paralysis
- Gliosis
- Neuronal loss in central nervous system
- Involuntary movements
- Drooling
And another 5 symptoms. If you need more information about this disease we can help you.
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.Amyotrophic Lateral Sclerosis 15 With Or Without Frontotemporal Dementia; Als15 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Amyotrophic Lateral Sclerosis Advanced Evaluation.
By Athena Diagnostics Inc (United States).
SOD1, SQSTM1, TARDBP, UBQLN2, VAPB, VCP, FIG4, OPTN, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, ANG, SIGMAR1, PFN1
Specificity
6 %
Genes
100 % |
Nonprevalent Amyotrophic Lateral Sclerosis Advanced Sequencing Evaluation.
By Athena Diagnostics Inc (United States).
SQSTM1, TARDBP, UBQLN2, VAPB, VCP, FIG4, OPTN, CHMP2B, DCTN1, FUS, ALS2, SETX, ANG, SIGMAR1, PFN1
Specificity
7 %
Genes
100 % |
Amyotrophic Lateral Sclerosis.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
ATXN2, SOD1, TARDBP, UBQLN2, VAPB, VCP, VEGFA, FIG4, OPTN, SPART, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, ANG, NEFH, SIGMAR1, PFN1 , (...)
View the complete list with 1 more genes
Specificity
5 %
Genes
100 % |
Amyotrophic lateral sclerosis 15 (sequence analysis of UBQLN2 gene).
By CGC Genetics (Portugal).
UBQLN2
Specificity
100 %
Genes
100 % |
Frontotemporal dementia (NGS panel for 13 genes).
By CGC Genetics (Portugal).
TARDBP, TUBA4A, UBQLN2, VCP, CHCHD10, CSF1R, CHMP2B, FUS, GRN, HNRNPA1, HNRNPA2B1, MAPT, PSEN1
Specificity
8 %
Genes
100 % |
Hereditary dementias (NGS panel for 28 genes).
By CGC Genetics (Portugal).
SNCA, SNCB, SORL1, TARDBP, TIMM8A, TUBA4A, TYROBP, UBQLN2, VCP, CHCHD10, TREM2, TRPM7, CSF1R, CHMP2B, DNMT1, ATP13A2, FUS, GRN, HNRNPA1, HNRNPA2B1 , (...)
View the complete list with 8 more genes
Specificity
4 %
Genes
100 % |
Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
SOD1, SQSTM1, TARDBP, TBK1, UBQLN2, VAPB, VCP, OPTN, CDH13, TREM2, CHMP2B, C9orf72, ARHGEF28, FUS, SETX, GRN, ANG, HNRNPA1, HNRNPA2B1, ANXA11 , (...)
View the complete list with 5 more genes
Specificity
4 %
Genes
100 % |
Amyotrophic Lateral Sclerosis via UBQLN2 Gene Sequencing with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
UBQLN2
Specificity
100 %
Genes
100 % |
You can get up to 32 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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