Type | Description |
---|---|
Definition | basic helix-loop-helix (bHLH) DNA-binding superfamily protein |
Date | Results | Publications |
---|---|---|
2019-05-18 10:56:00 | Mice with the DYT1 dystonia mutation exhibit an enhanced response to mu receptor activation, dependent on selective receptor gene upregulation.. | 29150865 |
2018-12-22 11:20:00 | Early onset torsion dystonia (DYT1) patient fibroblasts with heterozygous DYT1 mutant alleles showed decreased herpes simplex virus 1 plaque formation as compared to controls. | 29396398 |
2017-12-30 11:59:00 | DYT1 dystonia is a network disorder, with crucial nodes in sensory-motor integration of posterior parietal structures. | 27453152 |
2017-12-09 10:11:00 | The results of this study suggested that motor impairments in DYT1 KI animals only exhibit when the sensory stimuli are strongly altered during performance. | 27769743 |
2017-11-11 13:20:00 | Data said that the normal spatio-temporal subcellular localization of DYT1 is important for DYT1 function and/or that the BIF domains from different bHLH members might be functionally distinct. | 27113773 |
Type | IDs |
---|---|
Synonymous | DYSFUNCTIONAL TAPETUM 1, T6K22.60, T6K22_60 |
Gene |
UniProtKB-ID:
DYT1_ARATH
UniprotKB:
O81900
UniParc:
UPI00000A2CCD
EMBL:
EF637083,
AL031187,
AL161554,
CP002687
EnsemblGenome:
AT4G21330
KO:
ath:AT4G21330
|
Nucleutide sequences |
EMBL-CDS:
ABV21209.1,
CAA20198.1,
CAB79132.1,
AEE84442.1
Gene_ORFName:
T6K22.60
EnsemblGenome_TRS:
AT4G21330.1
|
Protein sequencees |
EnsemblGenome_PRO:
AT4G21330.1
RefSeq:
NP_193864.1
|
Others |
UniRef100:
UniRef100_O81900
UniRef90:
UniRef90_O81900
UniRef50:
UniRef50_O81900
UniGene:
At.54456
|
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