C3H101H-Mut1231/H
| Status | Available to order |
| EMMA ID | EM:01955 |
| Citation information | RRID:IMSR_EM:01955 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 | C3H101H-Mut1231/H |
| Alternative name | MUT/1231 |
| Strain type | Spontaneous |
| Allele/Transgene symbol | Mut1231 |
| Gene/Transgene symbol | Mut1231 |
Information from provider
| Provider | Bruce Cattanach |
| Provider affiliation | MRC Harwell, Didcot, Oxon, OX11 0RD |
| Genetic information | A spontaneous, dominant mutation which arose in the C3H/HeH x 101/H F1 stock at MRC Harwell. |
| Phenotypic information | Heterozygotes have curly whiskers and progressive hair loss commencing 8-12 days after birth by which time the skin is loose and wrinkled. By weaning most of the fur has gone from heterozygotes, by adulthood they are bald. Opening data are inconsistent, but suggest that some, if not all, homozygotes are lost pre-implantation. Openings from 3H1 females crossed to heterozygous males indicate little or no loss of Mut1231/+ prior to birth. Reciprocal openings suggest that heterozygous females have impaired ability to carry large litters to term. Viability of heterozygotes to weaning is good. Penetrance of the mutation on a 3H1 background and on outcrossing to Mus castaneus is also good. Mapping data (which position Mut1231 on Chr11) gave the following linkage: Cross 1: Mut1231 - 14.55 cM +/- 3.36 cM - Re. Cross 2: D11Mit1 - 30 cM +/- 6.48 cM - Mut1231 - 22 cM +/- 5.86 cM - D11Mit329. Intercrosses of mice heterozygous for both Mut1231 and Foxn1 failed to produce any phenotypically wild-type pups out of 213 offspring scored indicating that Mut1231 and Foxn1 are either allelic, or closely linked. Unlike Foxn1/Foxn1, Mut1231/+ mice are not athymic at weaning. |
| Breeding history | Mutation arose in the C3H/HeH x 101/H F1 stock at MRC Harwell. |
| References | None available |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).
