Gene Expression Literature Detail
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Symbol Name ID |
Diaph1
diaphanous related formin 1 MGI:1194490 |
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Reference
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J:228552 Ercan-Sencicek AG, Jambi S, Franjic D, Nishimura S, Li M, El-Fishawy P, Morgan TM, Sanders SJ, Bilguvar K, Suri M, Johnson MH, Gupta AR, Yuksel Z, Mane S, Grigorenko E, Picciotto M, Alberts AS, Gunel M, Sestan N, State MW, Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans. Eur J Hum Genet. 2015 Feb;23(2):165-72 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E12.5 | E14.5 | E17.5 | P |
| Immunohistochemistry (section) | ||||
| In situ RNA (section) | |
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| Immunohistochemistry (whole mount) | ||||
| In situ RNA (whole mount) | ||||
| In situ reporter (knock in) | ||||
| Northern blot | ||||
| Western blot | |
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| 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 11/12/2024 MGI 6.24 |
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