(Q14905729)

English

SCN5A

protein-coding gene in the species Homo sapiens

CDCD2
CMD1E
CMPD2
HB1
HB2
HBBD
HH1
ICCD
IVF
LQT3
Nav1.5
PFHB1
SSS1
VF1
sodium voltage-gated channel alpha subunit 5

In more languages

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000183873

Protein SCN5A PDB 1byy.png
730 × 392; 69 KB

0 references

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

Sodium voltage-gated channel alpha subunit 5

1 reference

6 July 2017

UniProt protein ID

genetic association

long QT syndrome 3

2 references

UniProt protein ID

13 August 2019

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/MONDO_0011377

based on heuristic

inferred from an Open Targets association score over 0.7

Brugada syndrome 1

1 reference

UniProt protein ID

13 August 2019

sudden infant death syndrome

2 references

UniProt protein ID

13 August 2019

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/EFO_0005303

based on heuristic

inferred from an Open Targets association score over 0.7

dilated cardiomyopathy 1E

1 reference

UniProt protein ID

13 August 2019

atrial fibrillation

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/EFO_0000275

based on heuristic

inferred from an Open Targets association score over 0.7

heart conduction disease

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/EFO_0004138

based on heuristic

inferred from an Open Targets association score over 0.7

heart arrhythmia

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/EFO_0004269

based on heuristic

inferred from an Open Targets association score over 0.7

idiopathic ventricular fibrillation, non Brugada type

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/MONDO_0011376

based on heuristic

inferred from an Open Targets association score over 0.7

Romano–Ward syndrome

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/Orphanet_101016

based on heuristic

inferred from an Open Targets association score over 0.7

progressive familial heart block

1 reference

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000183873/Orphanet_871

based on heuristic

inferred from an Open Targets association score over 0.7

human chromosome 3

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

38548057

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

38589548

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

38691164

human chromosome 3

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

38649687

human chromosome 3

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

cytogenetic location

3p22.2

1 reference

15 May 2022

22738

1 reference

15 May 2022

1 reference

HomoloGene build68

22738

1 reference

HomoloGene build68

22738

1 reference

HomoloGene build68

22738

1 reference

HomoloGene build68

22738

1

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

right ventricle

2

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

secondary oocyte

3

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

4

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

retinal pigment epithelium

5

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

ganglionic eminence

6

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

canal of the cervix

7

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

ascending aorta

8

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

gastrocnemius muscle

9

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

prefrontal cortex

10

1 reference

28 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000183873

http://identifiers.org/ncbigene/6331

1 reference

Identifiers.org

http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069

Identifiers

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

15 May 2022

Ensembl gene ID

ENSG00000183873

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

Ensembl transcript ID

ENST00000327956

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000333535

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000413689

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000414099

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000423572

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000449557

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000450102

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000455624

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000464652

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000476683

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

ENST00000491944

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000183873

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

Microsoft Academic ID

0 references

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(8 entries)

arwiki قناة الصوديوم Nav1.5
arzwiki قناة الصوديوم Nav1.5
bswiki SCN5A
dewiki SCN5A
enwiki SCN5A
fawiki Nav1.5
frwiki SCN5A
ukwiki SCN5A

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q14905729&oldid=1971198858"