Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | SCN3B | contributors: mct - updated : 15-09-2010 |
HGNC name | sodium channel, voltage-gated, type III, beta |
HGNC id | 20665 |
|
DNA |
TYPE | functioning gene |
STRUCTURE | 25.42 kb 7 Exon(s) |
10 Kb 5' upstream gene genomic sequence study |
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regulatory sequence | Binding site |
text structure | two putative p53-binding sites upstream of the first exon (RE1) and in the third intron (RE2) |
MAPPING | cloned | Y | linked | N | status | provisional |
RNA |
TRANSCRIPTS | type | messenger |
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|
EXPRESSION |
Type | restricted |
expressed in | (based on citations) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
organ(s) |
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tissue |
|
cells |
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cell lineage
cell lines
| fluid/secretion
| |
at STAGE |
physiological period | fetal |
Text | eye, brain |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
| |
motifs/domains
|
conjugated | GlycoP |
HOMOLOGY |
Homologene |
FAMILY |
CATEGORY | transport channel |
SUBCELLULAR LOCALIZATION | plasma membrane |
intracellular | |
intracellular,cytoplasm,organelle,endoplasmic reticulum |
basic FUNCTION | |
| |
|
CELLULAR PROCESS |
PHYSIOLOGICAL PROCESS |
PATHWAY |
metabolism |
signaling |
a component |
INTERACTION |
DNA |
RNA |
small molecule |
protein |
cell & other |
REGULATION |
ASSOCIATED DISORDERS |
corresponding disease(s) | BRGS7 , ATFB12 |
Other morbid association(s) |
|
Susceptibility | to atrial fibrillation |
Variant & Polymorphism other | A130V mutant SCN3B negated the function of wild type SCN3B, suggesting that A130V acts by a dominant negative mechanism in atrial fibrillation |
Candidate gene
Marker
| Therapy target
|
| |
ANIMAL & CELL MODELS |