Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | SCN5A | contributors: mct - updated : 04-09-2016 |
HGNC name | sodium channel, voltage-gated, type V, alpha subunit |
HGNC id | 10593 |
|
DNA |
TYPE | functioning gene |
STRUCTURE | 101.61 kb 28 Exon(s) |
10 Kb 5' upstream gene genomic sequence study |
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regulatory sequence | Promoter |
cytosine-phosphate-guanine/HTF | |
motif | repetitive sequence |
text structure | |
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MAPPING | cloned | Y | linked | N | status | confirmed |
RNA |
TRANSCRIPTS | type | messenger |
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EXPRESSION |
Type | restricted |
expressed in | (based on citations) | ||||||||||||||||||||||||||||||
organ(s) |
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tissue |
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cells |
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cell lineage
cell lines
| fluid/secretion
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at STAGE |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
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motifs/domains
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HOMOLOGY |
interspecies | homolog to murine Scn5a |
Homologene |
FAMILY |
CATEGORY | transport channel |
SUBCELLULAR LOCALIZATION | plasma membrane |
intracellular | |
intracellular,cytoplasm,organelle,membrane | |
intracellular,cytoplasm,organelle,endoplasmic reticulum | |
text | |
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basic FUNCTION |
CELLULAR PROCESS |
PHYSIOLOGICAL PROCESS |
PATHWAY |
metabolism |
signaling |
a component |
INTERACTION |
DNA |
RNA |
small molecule |
protein | |
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cell & other |
REGULATION |
ASSOCIATED DISORDERS |
corresponding disease(s) | LQT3 , PCCD2 , PCCD1 , SSS1 , CMD1E , BRGS1 |
related resource | Congenital Long QT Syndrome at GeneDis
Gene Connection for the Heart Long QT Syndrome Database |
Susceptibility | to cardiac arrhythmia and sudden death |
Variant & Polymorphism SNP , other | |
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Candidate gene
Marker
| Therapy target
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ANIMAL & CELL MODELS |