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Gene Expression Literature Detail
Symbol
Name
ID
Diaph1
diaphanous related formin 1
MGI:1194490

Reference
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

Detailed expression data for these assays: 36 results

red ball Indicates gene expression was analyzed but not necessarily detected.
Age E12.5 E14.5 E17.5 P
Immunohistochemistry (section)
In situ RNA (section) red ball red ball red ball red ball
Immunohistochemistry (whole mount)
In situ RNA (whole mount)
In situ reporter (knock in)
Northern blot
Western blot red ball
RT-PCR
cDNA clones
RNase protection
Nuclease S1
Primer Extension


Contributing Projects:
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
The Jackson Laboratory