Symbol Name ID |
Fam20c
FAM20C, golgi associated secretory pathway kinase MGI:2136853 |
Reference
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J:135966 Simpson MA, Hsu R, Keir LS, Hao J, Sivapalan G, Ernst LM, Zackai EH, Al-Gazali LI, Hulskamp G, Kingston HM, Prescott TE, Ion A, Patton MA, Murday V, George A, Crosby AH, Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development. Am J Hum Genet. 2007 Nov;81(5):906-12 |
Age | E15 | 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 | ||
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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