MGI phenotypes (allele matching)
C3H101HF1 x STOCK Del(13)80H +/+ Foxq1sa/H
| Status | Available to order |
| EMMA ID | EM:02211 |
| Citation information | RRID:IMSR_EM:02211 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 | C3H101HF1 x STOCK Del(13)80H +/+ Foxq1sa/H |
| Alternative name | Del(13)80H |
| Strain type | Induced Mutant Strains : Radiation-induced |
| Allele/Transgene symbol | Foxq1sa, Del(13)80H |
| Gene/Transgene symbol | Foxq1, Del(13)80H |
Information from provider
| Provider | Colin Beechey |
| Provider affiliation | MRC Harwell, Didcot, Oxon, OX11 0RD |
| Phenotypic information | Carriers are small with domed heads and small eyes. |
| References | None available |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI phenotypes (gene matching)
- decreased body size / MGI
- shiny fur / MGI
- abnormal head morphology / MGI
- decreased digestive secretion / MGI
- abnormal lymphocyte cell number / MGI
- abnormal brain development / MGI
- abnormal coat appearance / MGI
- abnormal hair growth / MGI
- abnormal hair texture / MGI
- abnormal response/metabolism to endogenous compounds / MGI
- abnormal hair shaft morphology / MGI
- abnormal hair cortex morphology / MGI
- abnormal hair medulla / MGI
- impaired natural killer cell mediated cytotoxicity / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI