MGI phenotypes (allele matching)
C3H.Cg-Foxq1sa Tas16/H
| Status | Available to order |
| EMMA ID | EM:01190 |
| Citation information | RRID:IMSR_EM:01190 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-Foxq1sa Tas16/H |
| Alternative name | TAS16 |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Tas16, Foxq1sa |
| Gene/Transgene symbol | Tas16, Foxq1 |
Information from provider
| Provider | Ruth Arkell |
| Provider affiliation | MRC Mammalian Genetics Unit |
| Genetic information | Mutant mice have a curly tail. |
| Phenotypic information | Curly tail in heterozygous (?) animals. |
| Breeding history | Original background: satin (Foxq1sa) on C3H/HeH partial congenic. Crossed to C3H/HeH for several generations. |
| References |
|
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI phenotypes (gene matching)
- 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
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