- abnormal organ of Corti morphology / MGI
- abnormal vascular development / MGI
- enlarged pericardium / MGI
- distended pericardium / MGI
- corneal opacity / MGI
- irregularly shaped pupil / MGI
- head bobbing / MGI
- impaired balance / MGI
- abnormal blood vessel morphology / MGI
- pale yolk sac / MGI
- hemorrhage / MGI
- intracranial hemorrhage / MGI
- abnormal eye morphology / MGI
- abnormal neural tube morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal semicircular canal morphology / MGI
- abnormal cochlear hair cell morphology / MGI
- head shaking / MGI
- abnormal posterior semicircular canal morphology / MGI
- no phenotypic analysis / MGI
- abnormal superior semicircular canal morphology / MGI
- abnormal vitelline vasculature morphology / MGI
- abnormal cochlear sensory epithelium morphology / MGI
- kinked neural tube / MGI
- embryonic growth retardation / MGI
- abnormal vitelline vascular remodeling / MGI
- abnormal crista ampullaris morphology / MGI
- increased cochlear inner hair cell number / MGI
- decreased cochlear outer hair cell number / MGI
- decreased neuronal precursor cell number / MGI
- head tossing / MGI
- positive geotaxis / MGI
- hearing/vestibular/ear phenotype / MGI
- embryonic lethality during organogenesis / MGI
- abnormal placement of pupils / MGI
- abnormal semicircular canal ampulla morphology / MGI
- increased neuron number / MGI
- abnormal neuron differentiation / MGI
- iris coloboma / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- embryo tissue necrosis / MGI
C3H;C-Jag1Ozz/H
| Status | Available to order |
| EMMA ID | EM:02210 |
| Citation information | RRID:IMSR_EM:02210 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | C3H;C-Jag1Ozz/H |
| Alternative name | GENA228 |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Jag1Ozz |
| Gene/Transgene symbol | Jag1 |
Information from provider
| Provider | Patrick Nolan |
| Provider affiliation | Medical Research Council |
| Phenotypic information | This mutation was identified during a dominant ENU mutagenesis screen. Mice carrying this mutation exhibit head weaving and circling behaviour. |
| References |
|
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Tetralogy of Fallot / Orphanet_3303
- Alagille syndrome due to a JAG1 point mutation / Orphanet_261619
MGI phenotypes (gene matching)
Literature references
- Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource.;Nolan P M, Peters J, Vizor L, Strivens M, Washbourne R, Hough T, Wells C, Glenister P, Thornton C, Martin J, Fisher E, Rogers D, Hagan J, Reavill C, Gray I, Wood J, Spurr N, Browne M, Rastan S, Hunter J, Brown S D, ;2000;Mammalian genome : official journal of the International Mammalian Genome Society;11;500-6; 10886012
Information on how we integrate external resources can be found here
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