Werner syndrome homolog (human) |
詳細情報を見る |
同義遺伝子名
Wrn, AI846146, Werner syndrome ATP-dependent helicase homolog, Werner syndrome homolog (human)
Refseq ID | NM_001122822 |
---|---|
Gene ID | 22427 |
Unigene ID | Mm.228805 |
Probe set ID | 1450163_a_at [Mouse430_2] |
Ensembl ID | ENSMUSG00000031583 |
8602509
8889548
9143515
9618508
9681877
9789047
10349636
10757074
10757812
10782115
10806190
10871373
10922068
11042159
11076861
11087671
11217851
11280729
11301316
11420665
11756244
11863428
12242664
12466851
12477932
12707040
12803543
12944467
14595844
14610273
15235603
15367665
15642393
15743673
16141072
16141073
16195394
16264192
16330174
16769258
16785251
17229737
18295300
18588880
18799693
19896421
20708636
21123451
21267068
21464516
22301954
22753033
8889548
9143515
9618508
9681877
9789047
10349636
10757074
10757812
10782115
10806190
10871373
10922068
11042159
11076861
11087671
11217851
11280729
11301316
11420665
11756244
11863428
12242664
12466851
12477932
12707040
12803543
12944467
14595844
14610273
15235603
15367665
15642393
15743673
16141072
16141073
16195394
16264192
16330174
16769258
16785251
17229737
18295300
18588880
18799693
19896421
20708636
21123451
21267068
21464516
22301954
22753033
Biological Process
Cellular Component
GO:0005813 | centrosome |
GO:0005622 | intracellular |
GO:0032389 | MutLalpha complex |
GO:0005730 | nucleolus |
GO:0005654 | nucleoplasm |
GO:0005634 | nucleus |