- increased circulating chloride level / IMPC
- abnormal spleen morphology / IMPC
- decreased spleen weight / IMPC
- decreased erythrocyte cell number / IMPC
- abnormal skin morphology / IMPC
- abnormal retina morphology / IMPC
- abnormal brain morphology / IMPC
- abnormal duodenum morphology / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased circulating total protein level / IMPC
- increased lean body mass / IMPC
- decreased effector memory T-helper cell number / IMPC
- enlarged heart / IMPC
- abnormal heart morphology / IMPC
- abnormal skeletal muscle morphology / IMPC
- enlarged testis / IMPC
- abnormal testis morphology / IMPC
- decreased lean body mass / IMPC
- hydrocephaly / IMPC
- decreased liver weight / IMPC
C3.C-Fbxl3Afh/H
| Status | Available to order |
| EMMA ID | EM:01841 |
| Citation information | RRID:IMSR_EM:01841 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 | C3.C-Fbxl3Afh/H |
| Alternative name | PLAY68 |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Fbxl3Afh |
| Gene/Transgene symbol | Fbxl3 |
Information from provider
| Provider | Pat Nolan |
| Provider affiliation | MRC Mammalian Genetics Unit |
| Phenotypic information | When maintained in cages equipped with wheels under constant darkness, heterozygotes have a longer circadian period (24.12-24.23 hours) than wild-type. |
| References |
|
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (gene matching)
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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