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20265 Scn1a

20265

Scn1a

sodium channel, voltage-gated, type I, alpha

protein-coding

Mus musculus

基因描述

Type Description
Definition sodium channel, voltage-gated, type I, alpha

研究结论

Date Results Publications
2021-02-06 13:58:00 Convulsive seizures and some behavioral comorbidities are uncoupled in the Scn1a(A1783V) Dravet syndrome mouse model. 32865826
2020-11-21 13:23:00 Adolescent behavioral abnormalities in a Scn1a(+/-) mouse model of Dravet syndrome. 31870807
2020-11-21 13:11:00 Delayed maturation of GABAergic signaling in the Scn1a and Scn1b mouse models of Dravet Syndrome. 30996233
2020-10-31 13:18:00 Epilepsy and neuropsychiatric comorbidities in mice carrying a recurrent Dravet syndrome SCN1A missense mutation. 31578435
2020-07-04 11:03:00 Findings forge a potential mechanistic link between impaired sharp-wave ripple (SPW-R) generation and Scn1a mutation in Dravet syndrome mice, expanding the set of disorders in which SPW-R dysfunction contributes to impaired memory. 31537705

名称对应

Type IDs
Synonymous B230332M13, Nav1.1
Gene
UniProtKB-ID: SCN1A_MOUSE
UniprotKB: A2APX8
UniParc: UPI0000604189, UPI0000604188, UPI0000604186
EMBL: AL928726, AL844526, AJ810515
Ensembl: ENSMUSG00000064329
KO: mmu:20265
Nucleutide sequences
EMBL-CDS: CAH17959.1
Ensembl_TRS: ENSMUST00000094951, ENSMUST00000077489, ENSMUST00000112366, ENSMUST00000112371
Protein sequencees
Ensembl_PRO: ENSMUSP00000107985, ENSMUSP00000076697, ENSMUSP00000107990, ENSMUSP00000092558
RefSeq: XP_006499090.1, XP_006499091.1, NP_061203.2, XP_036015705.1, NP_001300926.1
Others
UniRef100: UniRef100_A2APX8
UniRef90: UniRef90_A2APX8
UniRef50: UniRef50_P35498-2
UniGene: Mm.439704
CCDS: CCDS38131.1, CCDS84530.1

全选

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研究热度

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