Identity
HGNC
LOCATION
19q13.11
LOCUSID
ALIAS
ATFB13,BRGDA5,DEE52,EIEE52,GEFSP1
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 6324
MIM: 600235
HGNC: 10586
Ensembl: ENSG00000105711
Variants:
dbSNP: 6324
ClinVar: 6324
TCGA: ENSG00000105711
COSMIC: SCN1B
RNA/Proteins
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38139087 | 2023 | Impact of rs1805127 and rs55742440 Variants on Atrial Remodeling in Hypertrophic Cardiomyopathy Patients with Atrial Fibrillation: A Romanian Cohort Study. | 1 |
| 38139087 | 2023 | Impact of rs1805127 and rs55742440 Variants on Atrial Remodeling in Hypertrophic Cardiomyopathy Patients with Atrial Fibrillation: A Romanian Cohort Study. | 1 |
| 35603785 | 2022 | Neonatal Scn1b-null mice have sinoatrial node dysfunction, altered atrial structure, and atrial fibrillation. | 3 |
| 35801810 | 2022 | Association of sodium voltage-gated channel genes polymorphisms with epilepsy risk and prognosis in the Saudi population. | 1 |
| 35603785 | 2022 | Neonatal Scn1b-null mice have sinoatrial node dysfunction, altered atrial structure, and atrial fibrillation. | 3 |
| 35801810 | 2022 | Association of sodium voltage-gated channel genes polymorphisms with epilepsy risk and prognosis in the Saudi population. | 1 |
| 33901312 | 2021 | Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage-gated sodium channel function. | 7 |
| 33901312 | 2021 | Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage-gated sodium channel function. | 7 |
| 32503841 | 2020 | Sodium channel β1 subunits are post-translationally modified by tyrosine phosphorylation, S-palmitoylation, and regulated intramembrane proteolysis. | 7 |
| 32503841 | 2020 | Sodium channel β1 subunits are post-translationally modified by tyrosine phosphorylation, S-palmitoylation, and regulated intramembrane proteolysis. | 7 |
| 30386899 | 2019 | Abnormal Scn1b and Fxyd1 gene expression in the pulled-through ganglionic colon may influence functional outcome in patients with Hirschsprung's disease. | 2 |
| 30765606 | 2019 | Structures of human Na(v)1.7 channel in complex with auxiliary subunits and animal toxins. | 197 |
| 31729702 | 2019 | Clinical and genetic aspect of 30 tunisian families with febrile seizures. | 0 |
| 30386899 | 2019 | Abnormal Scn1b and Fxyd1 gene expression in the pulled-through ganglionic colon may influence functional outcome in patients with Hirschsprung's disease. | 2 |
| 30765606 | 2019 | Structures of human Na(v)1.7 channel in complex with auxiliary subunits and animal toxins. | 197 |
Citation
Dessen P
SCN1B (sodium voltage-gated channel beta subunit 1)
Atlas Genet Cytogenet Oncol Haematol. 2015-02-01
Online version: http://atlasgeneticsoncology.org/gene/54992/scn1b-(sodium-voltage-gated-channel-beta-subunit-1)
