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SCN5A
| Symbol: | SCN5A | | Name(s): | sodium channel, voltage-gated, type V, alpha subunit | | Type: | protein-coding | | Organism: | Homo sapiens | | Synonyms: | CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD, HH1, ICCD, IVF, LQT3, Nav1.5, PFHB1, SSS1 | | Links: |
Pubmed,
Entrez Gene,
GeneCards,
BioGPS,
Map Viewer.
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Gene Information from Publications |
| Publication Link |
Summary of findings |
| 18355654 |
Observational study of gene-disease association. (HuGE Navigator) |
| 18362431 |
Observational study of gene-disease association. (HuGE Navigator) |
| 18048769 |
the divergent biophysical defects caused by 2 different SCN5A mutations associated with familial dilated cardiomyopathy. |
| 18245395 |
SCN5A R1193Q polymorphism associated with progressive cardiac conduction defects and long QT syndrome in a Chinese family. |
| 11136691 |
Observational study of gene-disease association and gene-environment interaction. (HuGE Navigator) |
| 11289718 |
Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) |
| 11743032 |
Observational study of gene-disease association, genetic testing, and healthcare-related. (HuGE Navigator) |
| 11997281 |
Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) |
| 12106943 |
Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) |
| 14760488 |
Observational study of gene-disease association. (HuGE Navigator) | →View more information from publications. |
Recent Publications on SCN5A: |  |
Brugada syndrome ECG provoked by the selective serotonin reuptake inhibitor fluvoxamine.
A patient with an SCN5A p.W822X nonsense mutation, localized in the... | 31st October, 2009
| 1Institute of Clinical Pharmacology and Visceral Research, University of
| Europace. 2009 Oct 29.
DOI Direct Link |
Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy?
Summary We identified a patient with electrophysiologically verified... | 30th October, 2009
| SA Pathology at Women's and Children's Hospital, North Adelaide, SA,
| Epilepsia. 2009 Oct 27.
DOI Direct Link |
Sudden death: ethical and legal problems of post-mortem forensic genetic testing for hereditary cardiac diseases.
Elger BS, Michaud K, Fellmann F, Mangin P. Sudden death: ethical and legal... | 30th October, 2009
| Institut universitaire de medecine legale, Unite de droit medical et
| Clin Genet. 2009 Oct 23.
DOI Direct Link |
Mutations in sodium channel beta1- and beta2-subunits associated with atrial fibrillation.
BACKGROUND: We and others have reported mutations in the cardiac... | 30th October, 2009
| Department of Medicine, Vanderbilt University School of Medicine,
| Circ Arrhythm Electrophysiol. 2009 Jun;2(3):268-75. Epub 2009 Mar 6.
DOI Direct Link |
Tubulin polymerization modifies cardiac sodium channel expression and gating.
Aims: Treatment with the anticancer drug taxol (TXL), which polymerizes... | 29th October, 2009
| Heart Failure Research Center, Academic Medical Center, University of
| Cardiovasc Res. 2009 Oct 26.
DOI Direct Link |
→View more research publications. |
SCN5A results (if any) from reagent suppliers | 
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Antibodies to Sodium Channels
Scn5a(20271), rat, WB, pricing. S1946, Anti-Sodium Channel NaV1.5 human antibody produced in rabbit, (polyclonal), affinity isolated antibody ...
http://www.sigmaaldrich.com/etc/controller/controller-page.h...
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S8809 Monoclonal Anti-Sodium Channel, Pan antibody produced in ...
Scn10a(20264), Scn11a(24046), Scn1a(20265), Scn3a(20269), Scn4a(110880), Scn5a( 20271), Scn8a(20273), Scn9a(20274). shipped in, wet ice. storage temp. −20°C
...
https://www.sigmaaldrich.com/catalog/ProductDetail.do?N4=S88...
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Na+ CP type Vα (C-20) Antibody sc-23174
Species, Gene Name, Gene ID, Chromosome Location, Isoform (mRNA) Accession #, Protein Accession #, OMIM™ Number. Human, SCN5A, 6331, 3p22.2, NM_000335, ...
http://www.scbt.com/datasheet-23174-na-cp-type-valpha-c-20-a...
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Calcium Pump pan PMCA ATPase antibody [5F10] (ab2825) | Abcam
Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex. Proc Natl Acad Sci U S A 105:9355-60 ...
http://www.abcam.com/Calcium-Pump-pan-PMCA-ATPase-antibody-5...
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Citations Search
Notes: The authors investigated the interaction between the α1-syntrophin (SNTA1 ), and the α subunit (SCN5A) of the cardiac sodium channel macromolecular ...
http://www.promega.com/citations/default.aspx?citapp=protein...
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Sodium Channel Protein Antibody / Sodium Channel Protein Antibodies
Sodium Channel Protein Antibody / Sodium Channel Protein Antibodies.
http://www.scbt.com/zh/table-sodium_channel_protein.html...
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Na+ CP type Vα (C-20) Antibody sc-23174
Species, 遺伝子名, Gene ID, Chromosome Location, Isoform (mRNA) Accession #, Protein Accession #, OMIM™ Number. ヒト, SCN5A, 6331, 3p22.2, NM_000335, ...
http://www.scbt.com/ja/datasheet-23174-na-cp-type-valpha-c-2...
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