Type | Description |
---|---|
Definition | sodium channel, voltage-gated, type I, alpha |
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 |
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
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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