Type | Description |
---|---|
Definition | Werner syndrome RecQ like helicase |
Date | Results | Publications |
---|---|---|
2018-06-30 12:12:00 | These results suggest that a great number of endoplasmic reticulum (ER) gene products are regulated at the post-transcriptional level in the liver of Wrn mutant mice exhibiting an ER stress response. | 29494634 |
2016-09-10 11:26:00 | A mislocalization of the Wrn mutant protein in the liver endoplasmic reticulum fraction increased oxidative stress in that cellular compartment. Vitamin C reversed this oxidative stress. | 26521679 |
2016-06-04 10:41:00 | The deleterious effects of the helicase-deficient Wrn protein are mediated by the dysfunction of several cellular organelles. | 26447695 |
2015-10-31 11:27:00 | Data suggest that, in the context of Wrn deficiency-related telomere dysfunction, loss of p16Ink4a function could prevent cells from senescence. | 22754337 |
2015-04-11 12:16:00 | The FEN1 E359K germline mutation disrupts the FEN1-WRN interaction and FEN1 GEN activity, causing aneuploidy-associated cancers. | 24608430 |
Type | IDs |
---|---|
Synonymous | AI846146 |
Gene |
UniProtKB-ID:
WRN_MOUSE,
Q3TB25_MOUSE,
Q8BWH5_MOUSE
UniprotKB:
O09053,
Q3TB25,
Q8BWH5
UniParc:
UPI00005B27D5,
UPI0000023808,
UPI00000EA7C3
EMBL:
D86527,
AC115809,
AF241636,
BC060700,
AK171490,
AC153789,
D86526,
AK052466,
BC050921,
AF091215,
AF091216
Ensembl:
ENSMUSG00000031583
KO:
mmu:22427
|
Nucleutide sequences |
EMBL-CDS:
AAF64490.1,
BAA20270.1,
AAH60700.1,
AAC78077.1,
AAC72359.1,
AAH50921.1,
BAA20269.1,
BAE42489.1,
BAC35005.1
Ensembl_TRS:
ENSMUST00000033990,
ENSMUST00000033991
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000033990,
ENSMUSP00000033991
RefSeq:
XP_006509156.1,
XP_017168151.1,
XP_036009773.1,
NP_001116294.1,
NP_035851.3,
XP_006509154.1
|
Others |
UniRef100:
UniRef100_O09053
UniRef90:
UniRef90_O09053
UniRef50:
UniRef50_Q14191
UniGene:
Mm.228805
CCDS:
CCDS22229.1
|
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Refseq |
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