C57BL/6N-Antxr2em1(IMPC)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:13913 |
International strain name | C57BL/6N-Antxr2em1(IMPC)Wtsi/WtsiCnbc |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Antxr2em1(IMPC)Wtsi |
Gene/Transgene symbol | Antxr2 |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6N |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Juvenile hyaline fibromatosis / Orphanet_2028
- Infantile systemic hyalinosis / Orphanet_2176
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal uterus morphology / MGI
- abnormal uterine cervix morphology / MGI
- female infertility / MGI
- no phenotypic analysis / MGI
- lymphangiectasis / MGI
- abnormal miscarriage rate / MGI
- dilated vasculature / MGI
- reproductive system phenotype / MGI
- increased apoptosis / MGI
- pregnancy-related premature death / MGI
- abnormal myometrium morphology / MGI
- decreased sensitivity to induced cell death / MGI
- abnormal internal female genitalia morphology / MGI
- abnormal uterus physiology / MGI
- decreased susceptibility to bacterial infection induced morbidity/mortality / MGI
- parturition failure / MGI
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