MGI phenotypes (allele matching)
STOCK Foxq1sa M1645b/Foxq1+ M1645b+/H
| Status | Available to order |
| EMMA ID | EM:01852 |
| Citation information | RRID:IMSR_EM:01852 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 | STOCK Foxq1sa M1645b/Foxq1+ M1645b+/H |
| Alternative name | M1645B |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | M1645b, Foxq1sa |
| Gene/Transgene symbol | M1645b, Foxq1 |
Information from provider
| Provider | Ruth Arkell |
| Provider affiliation | MRC Mammalian Genetics Unit |
| Genetic information | Mutation occurring on mouse chromosome 13 (equivalent to human chromosome 6p21.3-23 and 6p25) which results in peri-implantation death. |
| Phenotypic information | Embryonic lethal. |
| 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
- Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse.;Arkell R M, Cadman M, Marsland T, Southwell A, Thaung C, Davies J R, Clay T, Beechey C V, Evans E P, Strivens M A, Brown S D, Denny P, ;2001;Mammalian genome : official journal of the International Mammalian Genome Society;12;687-94; 11641716