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| Caption | Urm1em1(IMPC)J/Urm1em1(IMPC)J (Urm1-/-) embryonic phenotype. Urm1-/- embryos are smaller than their littermates at E8.5 and display a range of phenotypes. While a minority of E8.5 Urm1-/- embryos appear normal as the embryo on the top, a minority are abnormal as the embryo in the middle, the majority of mutants are delayed (as the embryo on the bottom) when compared with littermates. At E9.5 almost all Urm1-/- embryos are delayed when compared with control littermates. Almost all E9.5 Urm1-/- embryos display incomplete turning and abnormal head shape, and most mutants appear to have abnormal branchial arches. Phenotypes present in half of E9.5 Urm1-/- embryos include abnormal cranial neural tube closure, abnormal cardiac development and slight neural tube kinking. By E10.5 Urm1-/- embryos that are not dying are all delayed and display abnormal head shape and slight neural tube kinking. | ||||
| Copyright | This image was contributed directly to MGI. Questions regarding this image or these data should be directed to Dr. Kimberly D. Tremblay at kdtrembl@umass.edu. J:374598 | ||||
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Associated Alleles |
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Associated Genotypes |
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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 01/06/2026 MGI 6.24 |
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