Type | Description |
---|---|
Definition | aprataxin |
Date | Results | Publications |
---|---|---|
2018-08-18 10:19:00 | Interaction with phosphorylated XRCC1 is a requirement for significant APTX recruitment to cellular DNA damage and enzymatic activity in cell extracts. | 29477978 |
2015-07-25 10:58:00 | Study demonstrates a protective role of Aptx in vivo and suggests that its loss results in progressive accumulation of DNA breaks in the nervous system, triggering hallmarks of premature ageing, systemically. | 25274775 |
2010-01-21 00:00:00 | neurological disorders associated with APTX mutations may be caused by the gradual accumulation of unrepaired DNA strand breaks resulting from abortive DNA ligation events | 16964241 |
2010-01-21 00:00:00 | aprataxin participates in chromosomal single-strand break repair | 19103743 |
Type | IDs |
---|---|
Synonymous | 2410016G21Rik, AA388047, FHA-HIT |
Gene |
UniProtKB-ID:
APTX_MOUSE
UniprotKB:
Q7TQC5
UniParc:
UPI0000003EA2,
UPI00000EB0D3,
UPI00000EA095,
UPI0000003EDB
EMBL:
AK088928,
BC021872,
AY040780,
AK005286,
AY208844,
AK010516,
AY040782,
AK077351
Ensembl:
ENSMUSG00000028411
KO:
mmu:66408
|
Nucleutide sequences |
EMBL-CDS:
AAK91771.1,
AAP86334.1,
AAK91773.1,
BAB26998.2,
BAB23933.2,
BAC40657.1,
BAC36763.1,
AAH21872.2
Ensembl_TRS:
ENSMUST00000030119,
ENSMUST00000108103,
ENSMUST00000068125
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000124264,
ENSMUSP00000030119,
ENSMUSP00000103738
RefSeq:
XP_006538234.1,
XP_011248386.1,
XP_006538233.1,
NP_001020615.1,
XP_036020202.1,
XP_030109558.1,
NP_079821.3,
NP_001020616.1,
XP_030109559.1,
XP_006538232.1,
XP_006538230.1,
XP_006538231.1,
XP_036020204.1
|
Others |
UniRef100:
UniRef100_Q7TQC5
UniRef90:
UniRef90_Q7TQC5
UniRef50:
UniRef50_Q7Z2E3
UniGene:
Mm.430710
CCDS:
CCDS38711.1,
CCDS38712.1
|
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