Gene Expression Literature Detail
|
Symbol Name ID |
Nr2f1
nuclear receptor subfamily 2, group F, member 1 MGI:1352451 |
|
Reference
|
J:294509 Bertacchi M, Gruart A, Kaimakis P, Allet C, Serra L, Giacobini P, Delgado-Garcia JM, Bovolenta P, Studer M, Mouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome. EMBO Mol Med. 2019 Aug;11(8):e10291 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | E11.5 | E12.5 | E13.5 | E18.5 | P |
| Immunohistochemistry (section) | |
|
|
|
|
|
| In situ RNA (section) | ||||||
| Immunohistochemistry (whole mount) | ||||||
| In situ RNA (whole mount) | ||||||
| In situ reporter (knock in) | ||||||
| Northern blot | ||||||
| Western blot | ||||||
| RT-PCR | ||||||
| cDNA clones | ||||||
| RNase protection | ||||||
| Nuclease S1 | ||||||
| Primer Extension |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 11/12/2024 MGI 6.24 |
|
|
|
||
Analysis Tools