Symbol Name ID |
Nr2f1
nuclear receptor subfamily 2, group F, member 1 MGI:1352451 |
Reference
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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 |
Age | E10.5 | E11.5 | E12.5 | E13.5 | E18.5 | P |
Immunohistochemistry (section) | ![]() |
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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) |
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last database update 08/02/2024 MGI 6.24 |
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