- 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 |
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 |
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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