Symbol Name ID |
Ror2
receptor tyrosine kinase-like orphan receptor 2 MGI:1347521 |
Reference
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J:119598 Oldridge M, Fortuna AM, Maringa M, Propping P, Mansour S, Pollitt C, DeChiara TM, Kimble RB, Valenzuela DM, Yancopoulos GD, Wilkie AO, Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B. Nat Genet. 2000 Mar;24(3):275-8 |
Age | E13 | E13.5 | E14 |
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 11/19/2024 MGI 6.24 |
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