Symbol Name ID |
Ercc2
excision repair cross-complementing rodent repair deficiency, complementation group 2 MGI:95413 |
Age | E7.5 | E16 | E17.5 | E18 | P |
Immunohistochemistry (section) | 1 | 1 | |||
In situ RNA (section) | 1 | 1 | 1 | ||
Western blot | 1 | ||||
cDNA clones | 1 |
Ercc2 excision repair cross-complementing rodent repair deficiency, complementation group 2 (Synonyms: Ercc-2, Mhdarco15, RCO015, XPD) | |
Results | Reference |
3* | J:93300 Blackshaw S, Harpavat S, Trimarchi J, Cai L, Huang H, Kuo WP, Weber G, Lee K, Fraioli RE, Cho SH, Yung R, Asch E, Ohno-Machado L, Wong WH, Cepko CL, Genomic analysis of mouse retinal development. PLoS Biol. 2004 Oct;2(9):E247 |
1 | J:50869 Ko MSH, Threat TA, Wang X, Horton JH, Cui Y, Pryor E, Paris J , Wells-Smith J , Kitchen JR , Rowe LB , Eppig J , Satoh T , Brant L , Fujiwara H , Yotsumoto S , Nakashima H, Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome. Hum Mol Genet. 1998 Nov;7(12):1967-78 |
2* | J:223515 Kunze S, Dalke C, Fuchs H, Klaften M, Rossler U, Hornhardt S, Gomolka M, Puk O, Sabrautzki S, Kulka U, Hrabe de Angelis M, Graw J, New mutation in the mouse xpd/ercc2 gene leads to recessive cataracts. PLoS One. 2015;10(5):e0125304 |
1 | J:129766 Sano M, Izumi Y, Helenius K, Asakura M, Rossi DJ, Xie M, Taffet G, Hu L, Pautler RG, Wilson CR, Boudina S, Abel ED, Taegtmeyer H, Scaglia F, Graham BH, Kralli A, Shimizu N, Tanaka H, Makela TP, Schneider MD, Menage-a-trois 1 is critical for the transcriptional function of PPARgamma coactivator 1. Cell Metab. 2007 Feb;5(2):129-42 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 12/10/2024 MGI 6.24 |
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