Gene Expression Literature Detail
|
Symbol Name ID |
Fat1
FAT atypical cadherin 1 MGI:109168 |
|
Reference
|
J:276459 Lahrouchi N, George A, Ratbi I, Schneider R, Elalaoui SC, Moosa S, Bharti S, Sharma R, Abu-Asab M, Onojafe F, Adadi N, Lodder EM, Laarabi FZ, Lamsyah Y, Elorch H, Chebbar I, Postma AV, Lougaris V, Plebani A, Altmueller J, Kyrieleis H, Meiner V, McNeill H, Bharti K, Lyonnet S, Wollnik B, Henrion-Caude A, Berraho A, Hildebrandt F, Bezzina CR, Brooks BP, Sefiani A, Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly. Nat Commun. 2019 Mar 12;10(1):1180 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | E11.5 | E12.5 |
| 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 12/10/2024 MGI 6.24 |
|
|
|
||
Analysis Tools