Symbol Name ID |
Dnaaf1
dynein, axonemal assembly factor 1 MGI:1915520 |
Reference
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J:158467 Loges NT, Olbrich H, Becker-Heck A, Haffner K, Heer A, Reinhard C, Schmidts M, Kispert A, Zariwala MA, Leigh MW, Knowles MR, Zentgraf H, Seithe H, Nurnberg G, Nurnberg P, Reinhardt R, Omran H, Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects. Am J Hum Genet. 2009 Dec;85(6):883-9 |
Age | E7.5 | E8 | E8.5 | E11.5 | E14.5 | E16.5 | E | 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) |
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last database update 12/17/2024 MGI 6.24 |
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