Gene Expression Literature Detail
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Symbol Name ID |
Asph
aspartate-beta-hydroxylase MGI:1914186 |
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Reference
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J:229861 Patel N, Khan AO, Mansour A, Mohamed JY, Al-Assiri A, Haddad R, Jia X, Xiong Y, Megarbane A, Traboulsi EI, Alkuraya FS, Mutations in ASPH cause facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs, or Traboulsi syndrome. Am J Hum Genet. 2014 May 1;94(5):755-9 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | E11.5 | E12.5 |
| Immunohistochemistry (section) | |
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| In situ RNA (section) | |||
| Immunohistochemistry (whole mount) | |||
| In situ RNA (whole mount) | |
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| 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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