| Type | Description |
|---|---|
| Definition | syntaxin 1B |
| Date | Results | Publications |
|---|---|---|
| 2021-01-02 12:51:00 | Epilepsy-causing STX1B mutations translate altered protein functions into distinct phenotypes in mouse neurons. | 32572454 |
| 2018-07-21 10:40:00 | Stx1b+/- mice exhibited reduced GABA release both in vitro and in vivo, disrupting the DAergic system in the CNS. Stx1b+/- mice exhibited reduced pre-pulse inhibition. | 29139159 |
| 2016-07-16 11:36:00 | Results demonstrated that STX1B is essential for the survival of neurons in vitro and it is a critical syntaxin protein for the neurotransmission at the mouse neuromuscular junctions | 26203110 |
| 2014-11-08 11:54:00 | Although STX1A and STX1B share a basic function as neuronal t-SNAREs, STX1B but not STX1A is necessary for the regulation of spontaneous and evoked synaptic vesicle exocytosis in fast transmission. | 24587181 |
| 2014-10-04 11:45:00 | STX1B was important for neuronal survival, possibly by regulating the secretion of neurotrophic factors | 24666284 |
| Type | IDs |
|---|---|
| Synonymous | Stx1b2, Stx1bl, Syn1b |
| Gene |
UniProtKB-ID:
STX1B_MOUSE
UniprotKB:
P61264
UniParc:
UPI0000000C13
EMBL:
D45207,
D29743,
BC132042,
BC132068,
AC149222
Ensembl:
ENSMUSG00000030806
KO:
mmu:56216
|
| Nucleutide sequences |
EMBL-CDS:
AAI32069.1,
BAA06162.1,
AAI32043.1,
BAA25986.1
Ensembl_TRS:
ENSMUST00000106267
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000101874
RefSeq:
XP_011240168.1,
XP_036009162.1,
XP_006508107.1,
NP_077725.1
|
| Others |
UniRef100:
UniRef100_P61266
UniRef90:
UniRef90_P61266
UniRef50:
UniRef50_P61266
UniGene:
Mm.439759
CCDS:
CCDS40146.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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