(Q14907685)

English

SCN9A

protein-coding gene in the species Homo sapiens

ETHA
FEB3B
GEFSP7
HSAN2D
NE-NA
NENA
Nav1.7
PN1
SFNP
sodium voltage-gated channel alpha subunit 9

In more languages

Statements

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

protein-coding gene

1 reference

Ensembl Release 87

Ensembl gene ID

ENSG00000169432

PDB 1byy EBI.jpg
500 × 290; 20 KB

0 references

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

Sodium voltage-gated channel alpha subunit 9

1 reference

6 July 2017

UniProt protein ID

genetic association

generalized epilepsy

determination method

genome-wide association study

1 reference

http://chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_216&ncbiId=6335

http://www.genome.gov/gwastudies/index.cfm?gene=SCN9A

Genome-wide association scan of dental caries in the permanent dentition

14 March 2017

Dravet syndrome

0 references

determination method

genome-wide association study

1 reference

https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_216&ncbiId=6335

http://www.genome.gov/gwastudies/index.cfm?gene=SCN9A

Genome-wide association scan of dental caries in the permanent dentition

25 May 2020

paroxysmal extreme pain disorder

2 references

UniProt protein ID

13 August 2019

Open Targets Platform

24 August 2023

https://platform.opentargets.org/evidence/ENSG00000169432/MONDO_0008179

based on heuristic

inferred from an Open Targets association score over 0.7

human chromosome 2

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

strand orientation

genomic assembly

genome assembly GRCh38

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

166195185

human chromosome 2

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

167051695

human chromosome 2

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

167232503

human chromosome 2

genomic assembly

Genome assembly GRCh37

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

166376001

human chromosome 2

genomic assembly

genome assembly GRCh38

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

cytogenetic location

2q24.3

1 reference

15 May 2022

2237

1 reference

15 May 2022

1 reference

HomoloGene build68

2237

1 reference

HomoloGene build68

2237

1

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

2

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

stromal cell of endometrium

3

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

trigeminal ganglion

4

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

Achilles tendon

5

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

right lobe of liver

6

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

7

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

8

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

transverse colon

9

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

islet of Langerhans

10

1 reference

20 April 2022

https://bgee.org/bgee15_0/gene/ENSG00000169432

http://identifiers.org/ncbigene/6335

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

ENSG00000169432

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

Ensembl transcript ID

ENST00000472119

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000303354

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000409672

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000452182

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000454569

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000645907

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000645815

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000642356

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000646694

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000645283

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000643319

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000667201

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

ENST00000667991

1 reference

ensembl Release 106

Ensembl gene ID

ENSG00000169432

0 references

HGNC gene symbol

1 reference

15 May 2022

1 reference

15 May 2022

1 reference

Online Mendelian Inheritance in Man

19 August 2019

1 reference

based on heuristic

inferred by common HGNC mappings on source and on Wikidata

15 June 2023

Sitelinks

Wikipedia(3 entries)

bswiki SCN9A
enwiki Nav1.7
ukwiki SCN9A

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)

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