scn1a.info

The SCN1A Infobase

Ool (Ver 1.8). A platform cataloging variations of the gene coding for the alpha-1 subunit (Na. 11) of neuronal voltage-gated sodium channels. This purpose of this web site is to provide an up-to-date compilation of genetic variations in the SCN1A. Gene that alter the expression or function of Na. 11 Associated phenotypes are mainly convulsive, including severe childhood epilepsies such as SMEI (Dravet syndrome), SMEB, ICEGTC, as well as more benign seizure disorders, like GEFS or FS.

http://www.scn1a.info/

OVERVIEW OF scn1a.info

TRAFFIC RANK

>1,000,000

REVIEWS

0

PAGES IN THIS WEBSITE

20

LINKS TO THIS WEBSITE

CONTACTS

ADDRESSES

SOCIAL LINKS

ONLINE SINCE

WEBSITE DETAILS

SEO

PAGES

SIMILAR SITES

TRAFFIC RANK FOR SCN1A.INFO

TODAY'S RATING

>1,000,000

TRAFFIC RANK - AVERAGE PER MONTH

BEST MONTH

March

AVERAGE PER DAY Of THE WEEK

HIGHEST TRAFFIC ON

Tuesday

TRAFFIC BY CITY

Sign up

CUSTOMER REVIEWS

Average Rating: 4.1 out of 5 with 17 reviews

5 star

8

4 star

5

3 star

3

2 star

0

1 star

1

Hey there! Start your review of scn1a.info

AVERAGE USER RATING

Write a Review

WEBSITE PREVIEW

LOAD TIME

0.5 seconds

FAVICON PREVIEW

16x16
32x32

CONTACTS AT SCN1A.INFO

UC Davis, Dept. Neurology

Christoph Lossin, Ph.D.

4635●●●● Ave

Sac●●●nto , CA, 95618

US

1.91●●●●5511

lo●●●●●@gmail.com

View this contact

Google, Inc.

Google Team

1600 Amp●●●●●●●● Parkway

Moun●●●●View , CA, 94043

US

1.●●50

ap●●●●●●●●●●@google.com

View this contact

UC Davis, Dept. Neurology

Christoph Lossin, Ph.D.

4635●●●● Ave

Sac●●●nto , CA, 95618

US

1.91●●●●5511

lo●●●●●@gmail.com

View this contact

Google, Inc.

Google Team

1600 Amp●●●●●●●● Parkway

Moun●●●●View , CA, 94043

US

1.●●50

ap●●●●●●●●●●@google.com

View this contact

ADD CONTACT

Login

TO VIEW CONTACTS

Remove Contacts

FOR PRIVACY ISSUES

DOMAIN REGISTRATION INFORMATION

REGISTERED: n/a
UPDATED: 2014 July 29
EXPIRATION: EXPIRED REGISTER THIS DOMAIN

BUY YOUR DOMAIN

NAME SERVERS

1: dns1.name-services.com
2: dns2.name-services.com
3: dns3.name-services.com
4: dns4.name-services.com
5: dns5.name-services.com

REGISTRAR

eNom, Inc. (R126-LRMS)

WHOIS : whois.afilias.info

REFERRED :

CONTENT

PAGES IN
THIS WEBSITE

20

SSL

EXTERNAL LINKS

1

SITE IP

64.233.171.121

LOAD TIME

0.502 sec

SCORE

6.2

PAGE TITLE

The SCN1A Infobase | scn1a.info Reviews

<META> DESCRIPTION

Ool (Ver 1.8). A platform cataloging variations of the gene coding for the alpha-1 subunit (Na. 11) of neuronal voltage-gated sodium channels. This purpose of this web site is to provide an up-to-date compilation of genetic variations in the SCN1A. Gene that alter the expression or function of Na. 11 Associated phenotypes are mainly convulsive, including severe childhood epilepsies such as SMEI (Dravet syndrome), SMEB, ICEGTC, as well as more benign seizure disorders, like GEFS or FS.

<META> KEYWORDS

1 the scn1a infobase

2 general

3 administration

4 news and updates

5 scn1a mutation data

6 exonic

7 non coding

8 genomic

9 polymorphisms

10 adjustments

CONTENT

Page content here

KEYWORDS ON PAGE

the scn1a infobase,general,administration,news and updates,scn1a mutation data,exonic,non coding,genomic,polymorphisms,adjustments,submit your data,general scn1a info,exon boundaries,topology,isoforms,promoter and utrs,phosphorylation sites,statistics

SERVER

GSE

CONTENT-TYPE

utf-8

GOOGLE PREVIEW

The SCN1A Infobase | scn1a.info Reviews

https://scn1a.info

Ool (Ver 1.8). A platform cataloging variations of the gene coding for the alpha-1 subunit (Na. 11) of neuronal voltage-gated sodium channels. This purpose of this web site is to provide an up-to-date compilation of genetic variations in the SCN1A. Gene that alter the expression or function of Na. 11 Associated phenotypes are mainly convulsive, including severe childhood epilepsies such as SMEI (Dravet syndrome), SMEB, ICEGTC, as well as more benign seizure disorders, like GEFS or FS.

INTERNAL PAGES

scn1a.info

1

Polymorphisms - The SCN1A Infobase

http://www.scn1a.info/Polymorphisms

Ool (Ver 1.8). Note: Some of the variants listed here involve more than one base, so we chose to title this page "Polymorphisms" rather than "Single nucleotide polymorphisms (SNPs)". Exon-intron boundaries were deduced from rat Scn1a using NCBI's Basic Local Alignment Tool. BLAST). An effort was made to reference the first report of the mutation. Topological data are taken from the secondary structure suggested in Escayg and colleagues in 2000.

2

Glossary - The SCN1A Infobase

http://www.scn1a.info/glossary

Ool (Ver 1.8). GEFS : generalized epilepsy with febrile seizures, plus ( OMIM #604233. ICEGTC: intractable childhood epilepsy with generalized tonic-clonic seizures; debated as a variant of SMEI. SMEB: a phenotypic variant of SMEI where patients lack one or more clear components of classic SMEI. SMEI: severe myoclonic epilepsy in infancy or Dravet's syndrome ( OMIM #607208. Http:/ www.scn1a.info.

3

Phosphorylation sites - The SCN1A Infobase

http://www.scn1a.info/phosphorylation

Ool (Ver 1.8). Mass-spec analysis reveals phosphorylation sites in Na. Berendt and co-workers published a manuscript in the Journal of Proteome Research that looked at phosphorylation in brain Na. 1x channels using affinity purification, tryptic digestion, and mass spec of the generated peptides ( J Proteome Res, EPub 23Feb2010, PMID: 20131913. The antigenicity of the antibodies was such that one was highly selective for Na. 12 (96 % selective vs other Na. S), while the second antibody detected all Na.

4

Antibodies - The SCN1A Infobase

http://www.scn1a.info/Antibodies

Ool (Ver 1.8). There are several Na. 11 antibodies available from commercial sources. All of the following information compares the antibody properties against the protein sequence for human full-length Na. 11 based on Accession Number P35498. Raised against: 1502-1519 of rat Na. 11[full]: 1502-1519 of human Nav1.1 (100 % match). 11[full]: not yet checked. WARNING - likely cross reactivity with human Na. 19 based on 100 % sequence match ( NM 014139. Other paralogs not checked. Does not carry a Na.

5

MAT - Mutation Analysis Tool - The SCN1A Infobase

http://www.scn1a.info/MAT

Ool (Ver 1.8). MAT - Mutation Analysis Tool. H ow will the base pair change you've discovered change the amino acid sequence of Nav1.1? Is the mutation you're looking at an in-frame deletion? Or an in-frame insertion? Does it affect splicing? Where does a particular base-pair exchange locate to in the topology of the channel? Has the mutation been reported before? What is the nucleic acid basis for a mutation that has only been reported at the amino acid level? Any mutation in SCN1A. New "Reverse Substit...

UPGRADE TO PREMIUM TO VIEW 15 MORE

TOTAL PAGES IN THIS WEBSITE

20

LINKS TO THIS WEBSITE

dravetdata.com

DravetData.com: SCN1A Articles & Research

http://www.dravetdata.com/scn1a.htm

Dravet and Epilepsy News Feeds. What is Dravet Syndrome? SCN1A Articles and Research. 242 out of 333 (73%) patients with Dravet Syndrome where found to have SCN1A mutations or deletions, 228 patients were found to have point deletions and of those 161 had mutations that where not previously reported. (26 September 2008) fact from. So to clarify - Not all Dravet Syndrome patients will have a SCN1A mutation. SCN1A mutations can also be found in conditions other then Dravet Syndrome (I.e. GEFS ). Spectrum o...

UPGRADE TO PREMIUM TO VIEW 0 MORE

TOTAL LINKS TO THIS WEBSITE

1

OTHER SITES

scn15.skyrock.com

Blog de SCN15 - Blog de SCN15 - Skyrock.com

Mot de passe :. J'ai oublié mon mot de passe. Mise à jour :. You Can't Always Get What You (Let It Bleed). Abonne-toi à mon blog! N'oublie pas que les propos injurieux, racistes, etc. sont interdits par les conditions générales d'utilisation de Skyrock et que tu peux être identifié par ton adresse internet (54.145.69.42) si quelqu'un porte plainte. Ou poster avec :. Retape dans le champ ci-dessous la suite de chiffres et de lettres qui apparaissent dans le cadre ci-contre. Ou poster avec :. N'oublie pas ...

scn1815-celle.de

Schützencorps Neuenhäusen von 1815 e.V. Celle

scn1901.com

web1248 @ susanne.webhoster.ag

Hier entstehen die Internet-Seiten des Confixx Benutzers web1248. Auf susanne.webhoster.ag.

scn1980ev.de

Segel- und Surfclub Niedernberg 1980 e.V.

Segel- und Surfclub Niedernberg 1980 e.V. Katamaran-Regatta Sonntag 23.08.2015. Liebe Mitglieder des SCN,. Am 23 August findet die erste Katamaran-Regatta auf dem Silbersee statt. Zu dieser vereinsinternen Regatta rufe ich alle unsere Katamaran-Segler zur Teilnahme auf. Wer gerne bei einem Kat als Vorschoter mitsegeln möchte, kann sich gerne melden. Vielleicht hat der eine oder andere noch einen Platz zum Mitsegeln. Start der Regatta um 11 Uhr, Ende je nach Windverhältnisen ca. 17 Uhr. Bei Auswahl wählt ...

scn1992.wordpress.com

SCN1992 | Hersenspinsels van mij!

Het mooiste dat je kunt worden, is jezelf. On: oktober 26, 2011. Deze spreuk las ik ergens, heb ik niet zelf bedacht. Maar wat vond ik hem mooi. Want het is waar. Je kan topchef willen worden, profvoetballer, sociaal pedagoog, timmerman of putjesschepper, het is allemaal niks waard zolang je jezelf niet kent en bent. En ken ik mezelf eigenlijk? Want je kan wel een goede baan hebben en lekker veel geld verdienen, wat heb je eraan als je niet lekker in je vel zit en niet kunt zijn wie je wilt. Stop met...

scn1a.info

The SCN1A Infobase

Ool (Ver 1.8). A platform cataloging variations of the gene coding for the alpha-1 subunit (Na. 11) of neuronal voltage-gated sodium channels. This purpose of this web site is to provide an up-to-date compilation of genetic variations in the SCN1A. Gene that alter the expression or function of Na. 11 Associated phenotypes are mainly convulsive, including severe childhood epilepsies such as SMEI (Dravet syndrome), SMEB, ICEGTC, as well as more benign seizure disorders, like GEFS or FS.

scn2000.livejournal.com

The Dog Photographer

And other assorted subjects. Arizona border collie rescue. Border collie / aussie mix puppy. Casey the talking dog. Fiesta cluster dog shows. National canine cancer foundation. We are the cure. Zen of tennis ball. Turner the 6 month old Irish. Beans, Books and Barks Paw Patio opening. AKA, my Saturday. A Hiking we will go. Duncan, My Heart. Where's the Border Collie? The bath before show day. Arizona Border Collie Rescue Calendar. Summer Vacation - Our Dog Talks! Powered by LiveJournal.com. Apr 18th, 2008.

scn2004er.de

SC Neheim U13 Jahrgang 2004 - scn2004er

Termine / Berichte / Archiv / Fotos. Termine / Berichte / Archiv / Fotos. Willkommen auf unserer Homepage. Hier findet ihr Informationen zur 2004er Mannschaft des SC Neheim. Diese Homepage ist rein privat und nicht im Auftrag des SC Neheim entstanden*. Rechtschreibfehler sind beabsichtigt und dienen der allgemeinen Belustigung. Wer einen findet darf ihn behalten. Aktualisiert am 12.01.). RAINER S CORNER auf Google Drive. Dies ist eine rein private Homepage. Diese Webseite verwendet Cookies.

scn2009.at

Home

20 Int. Halbmarathon Stinatz,. 23 Lauf zum Österreichischen Volkslaufcup. Dieses Wochenende ging die Reise für die SC Neustift im Felde Sportler in das Burgenland nach Stinatz. Mit von der Partie waren Valentina, Samuel, Lea, Josef. Startete im Knirpsenlauf über 300m wo ohne Zeit und Platzierung gelaufen wurde. In der Altersklasse Männlich U10 war Samuel Jamöck. Weiterlesen: Podestplätze im Burgenland. 11 WERBEPROFI-Schlossparklauf in Gmünd. Waldviertler Laufcup, 7von 11 Läufen. Die zweite im Bunde war L...

scn21.com

南京赛诚制冷设备有限公司【官方网站】

北京时间10月31日消息，据国外媒体报道，美国股神沃伦·巴菲特(WarrenBuffett)近日接受了美国CNBC电视台S. 南京赛诚制冷设备有限公司南京新赛厨具设备有限公司，位于南京市溧水东屏工业园，毗邻南京禄口国际机场，紧邻中国第一大港口上海港，地理位置优越. [查看详细]. G2-A系列冰淇淋展示柜 2014款简称14款，此款冰淇淋柜是为了适应国外市场的需求在G1-A系列老款的基础上对结.

scn2222.com

山村侬(磐安特产),磐安香菇之乡欢迎您

Pan An Village Agricultural Specialty Co.ltd. 磐安山村农特产有限公司是以生产、加工、销售食用菌为一体的农产品加工企业，主要经营香菇、杏鲍菇、木耳、灰树花、鸡腿菇、巴西菇、滑子菇、牛肝菌、茶树菇、天麻、小京生等家特产,品种多样,价格优惠,质量上乘. 公司理念:顾客满意是我的心愿.坚持"诚信为本、质量第一、顾客至上的宗旨欢迎新老客刻选购山村农特? 玩具木屑种香菇云和两大产业联姻结硕果. ƻ ٹ ahao20131217 Űټ. ƻ ٹ ahao20131217UTF 澳门百家乐. X6FB3;门博彩网. X6FB3;门博彩网站. X6FB3;门博彩网址. X6FB3;门赌博. X6FB3;门赌场. X6FB3;门现金网. X767E;家乐. X767E;家乐开户. X535A;彩评级. X8D4C;博网. X8D4C;博网站. X7F51;上赌博. X73B0;金赌博. X73B0;金网. X73B0;金游戏. X5A31;乐城. X771F;人博彩. X771F;人娱乐.