- prenatal lethality, complete penetrance / MGI
- abnormal cartilage development / MGI
- decreased cell proliferation / MGI
- decreased embryo size / MGI
- edema / MGI
- spina bifida / MGI
- pallor / MGI
- embryonic growth retardation / MGI
- decreased fetal size / MGI
- small cranium / MGI
- hearing/vestibular/ear phenotype / MGI
- cardiovascular system phenotype / MGI
- abnormal skeleton morphology / MGI
- abnormal limb development / MGI
- small thoracic cage / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- decreased fibroblast proliferation / MGI
- decreased bone ossification / MGI
- open neural tube / MGI
- abnormal embryonic growth/weight/body size / MGI
129S5.Cg-Med31l11Jus15 +/+ In(11Trp53;11Wnt3)8Brd/H
Status | Available to order |
EMMA ID | EM:04964 |
Citation information | RRID:IMSR_EM:04964 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 | 129S5.Cg-Med31l11Jus15 +/+ In(11Trp53;11Wnt3)8Brd/H |
Alternative name | Med31l11Jus15 |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | Med31l11Jus15, In(11Trp53;11Wnt3)8Brd |
Gene/Transgene symbol | Med31, In(11Trp53;11Wnt3)8Brd |
Information from provider
Provider | Kathryn Hentges |
Provider affiliation | Paterson Institute for Cancer Research, University of Manchester |
Additional owner | Prof. Monica Justice, Baylor College of Medicine, Houston, Texas, USA |
Genetic information | ENU induced point mutation in Med31 causing premature stop codon. Truncated protein is unstable. |
Phenotypic information | Embryonic lethality with reduced cell proliferation rates in embryonic fibroblasts. |
Breeding history | Outcrossed 8 generations to 129S5. Maintained as balanced stock with chromosome 11 balancer chromosome described in Kile et al., 2003 Nature 425:81-6. |
References | None available |
Homozygous fertile | no |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Animals used for archiving | heterozygous 129S5/SvEvBrd males |
Breeding at archiving centre | Males were archived upon arrival at the archiving centre. No breeding was performed. |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal cartilage development / MGI
- decreased cell proliferation / MGI
- open neural tube / MGI
- decreased embryo size / MGI
- edema / MGI
- abnormal embryonic growth/weight/body size / MGI
- spina bifida / MGI
- pallor / MGI
- embryonic growth retardation / MGI
- decreased fetal size / MGI
- small cranium / MGI
- hearing/vestibular/ear phenotype / MGI
- cardiovascular system phenotype / MGI
- abnormal skeleton morphology / MGI
- abnormal limb development / MGI
- small thoracic cage / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- decreased fibroblast proliferation / MGI
- decreased bone ossification / MGI
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