- decreased cell proliferation / MGI
- open neural tube / MGI
- abnormal embryo development / MGI
- reduced fertility / MGI
- decreased litter size / MGI
- abnormal tail morphology / MGI
- abnormal neural tube morphology / MGI
- no abnormal phenotype detected / MGI
- delayed neural tube closure / MGI
- vestigial tail / MGI
- curly tail / MGI
- abnormal neural tube closure / MGI
- failure of eyelid fusion / MGI
- delayed eyelid fusion / MGI
- neonatal lethality, incomplete penetrance / MGI
- abnormal caudal neuropore morphology / MGI
- spina bifida cystica / MGI
- incomplete caudal neuropore closure / MGI
STOCK Axd/Cnrm
Status | Available to order |
EMMA ID | EM:02424 |
Citation information | RRID:IMSR_EM:02424 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 Axd/Cnrm |
Alternative name | BALB/c - Axial defects |
Strain type | Spontaneous |
Allele/Transgene symbol | Axd |
Gene/Transgene symbol | Axd |
Information from provider
Provider | Madeleine BROUNS |
Provider affiliation | Maastricht University |
Genetic information | Unknown. |
Phenotypic information | All homozygotes display curled tails and/or spina bifida. 40% of heterozygotes displays curled tails. Homozygous animals have reduced fertility. |
Breeding history | Rederived heterozygous Axial defects mice were crossed 3 consecutive times with BALB/c while selecting the dominant curled tail phenotype. Genetic background was monitored using polymorphic marker analysis. This speed congenics protocol resulted in 95% BALB/c genetic background as assessed by 63 markers evenly spread over the genome. Currently the strain is bred as a heterozygous line, maintained by crosses with wild type mice of the same genetic background. Heterozygotes are identified by their curled tail phenotype. |
References |
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Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
MGI phenotypes (gene matching)
Literature references
- Expression of a new mutation (Axd) causing axial defects in mice correlates with maternal phenotype and age.;Essien F B, Haviland M B, Naidoff A E, ;1990;Teratology;42;183-94; 2218945
- Maternal methionine supplementation promotes the remediation of axial defects in Axd mouse neural tube mutants.;Essien F B, ;1992;Teratology;45;205-12; 1615430
- Methionine but not folinic acid or vitamin B-12 alters the frequency of neural tube defects in Axd mutant mice.;Essien F B, Wannberg S L, ;1993;The Journal of nutrition;123;27-34; 8421227
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