- abnormal snout morphology / IMPC
- abnormal startle reflex / IMPC
- increased circulating HDL cholesterol level / IMPC
- increased lean body mass / IMPC
- increased circulating cholesterol level / IMPC
- decreased circulating cholesterol level / IMPC
- decreased circulating amylase level / IMPC
- increased total body fat amount / IMPC
- preweaning lethality, complete penetrance / IMPC
C3H.Cg-Celsr1Scy/H
| Status | Available to order |
| EMMA ID | EM:00084 |
| Citation information | RRID:IMSR_EM:00084 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.Cg-Celsr1Scy/H |
| Alternative name | GENA175 |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Celsr1Scy |
| Gene/Transgene symbol | Celsr1 |
Information from provider
| Provider | Pat Nolan |
| Provider affiliation | MRC Mammalian Genetics Unit |
| Phenotypic information | Mice carrying this mutation exhibit circling behaviour. |
| References |
|
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal head morphology / IMPC
- male infertility / IMPC
- female infertility / IMPC
- abnormal brain morphology / IMPC
- abnormal spleen morphology / IMPC
- enlarged testis / IMPC
- cataract / IMPC
- increased brain size / IMPC
- increased total body fat amount / IMPC
- abnormal tail morphology / IMPC
- enlarged spleen / IMPC
- abnormal snout morphology / IMPC
- no spontaneous movement / IMPC
- increased lean body mass / IMPC
- abnormal skin morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- corneal opacity / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- increased circulating HDL cholesterol level / IMPC
- abnormal startle reflex / IMPC
- increased circulating cholesterol level / IMPC
- decreased lean body mass / IMPC
- abnormal retina morphology / IMPC
- abnormal testis morphology / IMPC
- abnormal vitreous body morphology / IMPC
- decreased circulating cholesterol level / IMPC
- decreased circulating amylase level / IMPC
- necrosis / IMPC
MGI phenotypes (allele matching)
- craniorachischisis / MGI
- spinning / MGI
- head shaking / MGI
- abnormal cochlear sensory epithelium morphology / MGI
- abnormal organ of Corti supporting cell morphology / MGI
- cochlear outer hair cell degeneration / MGI
- abnormal orientation of outer hair cell stereociliary bundles / MGI
- head bobbing / MGI
- abnormal involuntary movement / MGI
- incomplete rostral neuropore closure / MGI
- absent eyelids / MGI
- abnormal outer hair cell kinocilium morphology / MGI
- perinatal lethality, complete penetrance / MGI
MGI phenotypes (gene matching)
- abnormal hair follicle orientation / MGI
- ruffled hair / MGI
- kinked tail / MGI
- cranioschisis / MGI
- incomplete rostral neuropore closure / MGI
- open neural tube / MGI
- abnormal lung morphology / MGI
- pulmonary hypoplasia / MGI
- decreased body size / MGI
- absent eyelids / MGI
- circling / MGI
- head bobbing / MGI
- spinning / MGI
- abnormal coat appearance / MGI
- increased susceptibility to otitis media / MGI
- hydroencephaly / MGI
- reduced fertility / MGI
- deafness / MGI
- prenatal lethality / MGI
- delayed neural tube closure / MGI
- head shaking / MGI
- curly tail / MGI
- testicular atrophy / MGI
- abnormal cochlear sensory epithelium morphology / MGI
- abnormal involuntary movement / MGI
- small lung / MGI
- abnormal neural tube closure / MGI
- abnormal organ of Corti supporting cell morphology / MGI
- abnormal respiratory conducting tube morphology / MGI
- cochlear outer hair cell degeneration / MGI
- abnormal orientation of outer hair cell stereociliary bundles / MGI
- head tossing / MGI
- abnormal neural plate morphology / MGI
- dilated terminal bronchiole tubes / MGI
- impaired hearing / MGI
- abnormal lung epithelium morphology / MGI
- craniorachischisis / MGI
- whorled hair / MGI
- abnormal lung saccule morphology / MGI
- abnormal lung lobe morphology / MGI
- small lung lobe / MGI
- abnormal branching involved in lung morphogenesis / MGI
- impaired branching involved in terminal bronchiole morphogenesis / MGI
- abnormal outer hair cell kinocilium morphology / MGI
- perinatal lethality, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- thick lung-associated mesenchyme / MGI
- increased or absent threshold for auditory brainstem response / MGI
Literature references
- A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.;Nolan P M, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray I C, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson J A, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel K P, Voegeling S, Guenet J L, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher E M, Martin J, Rastan S, Brown S D, Hunter J, ;2000;Nature genetics;25;440-3; 10932191
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