Talk:SCN2A

OMIM changed

new number: 182390 --JWSchmidt (talk) 23:24, 25 December 2010 (UTC)

Other places where SCN2A is mentioned on Wikipedia

Let's consider linking to these pages in the SCN2A protein article.

Mentioned in main article

1. International SCN2A Awareness Day
2. Generalized Epilepsy with Febrile Seizures Plus - SCN2A Mutations
3. Dravet Syndrome

Mentioned in references / needs updated information

1. Syndromic Autism
2. Wendy Chung

Jorditty (talk) 14:07, 22 November 2025 (UTC)

Here's the full list from a search with the terms "SCN2A related disorder":

https://en.wikipedia.org/w/index.php?search=SCN2A+related+disorder&title=Special%3ASearch&ns0=1

The page "SCN2A related disorder" does not exist. You can click on "SCN2A related disorder" to create the page directly, or you may create a draft and submit it for review, but consider checking the search results below to see whether the topic is already covered.

• International SCN2A Awareness Day FamilieSCN2A Foundation, SCN2A Australia, SCN2A Brasil, SCN2A Georgia, SCN2A Europe, SCN2A Foundation, SCN2A Germany e.V., SCN2A Italia, SCN2A UK, and SCN2A... 18 KB (1,662 words) - 17:04, 19 November 2025
• SCN2A spectrum disorders and/or developmental delay, called SCN2A-related disorders. The SCN2A gene is composed of 27 exons and comprises more than 150 kilobases... 22 KB (2,091 words) - 13:39, 19 November 2025
• Syndromic autism (redirect from Monogenic autism spectrum disorder) isodicentric 15q) Autism-associated genes (e.g., ADNP, ARIDB1B, ANK2, SCN2A, KCNH1) Autism-associated CNVs (e.g., 16p11.2 deletion/duplication, exonic... 18 KB (1,180 words) - 22:24, 13 November 2025
• List of genetic disorders The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene"... 43 KB (995 words) - 16:21, 17 November 2025
• Generalized epilepsy with febrile seizures plus (section SCN2A mutations) another gene related with calcium channel the PCDH19 which is also known as Epilepsy Female with Mental Retardation. Penetrance for this disorder is estimated... 35 KB (3,419 words) - 15:18, 1 November 2025
• Dravet syndrome (category Neurological disorders in children) gene does not necessarily mean that the patient has Dravet syndrome. - SCN2A: This gene encodes the alpha-2 subunit of the sodium ion channel (Nav1.2)... 34 KB (4,120 words) - 23:33, 27 October 2025
• Wendy Chung (section Autism and neurodevelopmental disorders) Kevin J. (2018-07-01). "Progress in Understanding and Treating SCN2A-Mediated Disorders". Trends in Neurosciences. 41 (7): 442–456. doi:10.1016/j.tins... 41 KB (3,844 words) - 16:23, 18 November 2025
• Ohtahara syndrome (category Neurological disorders) ARHGEF9, PCDH19, PNKP, SCN2A, PLCB1, SCN8A, ST3GAL3, TBC1D24, BRAT1 and likely others. Less often, the root of the disorder is an underlying metabolic... 16 KB (1,509 words) - 15:18, 1 November 2025
• Mechanism of autism and development of the synapse. Some of those implicated include SHANK3, SCN2A, and PTEN. Neuroanatomical studies and the association between autism and... 63 KB (6,896 words) - 15:57, 5 October 2025
• Epilepsy syndromes (section Febrile infection-related epilepsy syndrome) self-limited neonatal epilepsy, PRRT2 or less commonly SCN2A or SCN8A in self-limited infantile epilepsy and SCN2A or KCNQ2 in self-limited neonatal-infantile epilepsy... 44 KB (5,705 words) - 15:17, 1 November 2025
• Lennox–Gastaut syndrome (category Neurological disorders) novo mutations in a variety of genes, including CHD2, GABRB3, ALG13 and SCN2A. The Epi4K study consortium (2013) observed de novo mutations in at least... 33 KB (3,629 words) - 17:26, 17 November 2025
• SCN3A Nishizaki K, Meyer NC, Smith RJ (February 2001). "Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus". Gene. 264... 8 KB (1,055 words) - 18:16, 17 July 2025
• Joseph Buxbaum  ; Buxbaum, J. D.; Meisler, M. H. (2003-02-01). "Sodium channels SCN1A, SCN2A and SCN3A in familial autism". Molecular Psychiatry. 8 (2): 186–194. doi:10... 22 KB (2,421 words) - 14:43, 30 September 2025
• Paralytic (gene) properties of sodium channels. The most closely related genes to paralytic in humans are SCN1A, SCN8A and SCN2A, all of which are genes that encode sodium... 9 KB (981 words) - 07:54, 22 June 2024
• Sodium channel linked to multiple severe developmental disorders and cervical dystonia. Schizophrenia and bipolar disorder are also linked to mutations to NALCN. Changes... 53 KB (5,675 words) - 16:27, 27 October 2025

Jorditty (talk) 14:14, 22 November 2025 (UTC)

SCN2A protein image

The original image was incorrect; updated with new image. Jorditty (talk) 21:03, 14 May 2026 (UTC)