- decreased presacral vertebrae number / MGI
- increased rib number / MGI
- abnormal forelimb morphology / MGI
- abnormal hindlimb morphology / MGI
- polydactyly / MGI
- oligodactyly / MGI
- abnormal uterus morphology / MGI
- abnormal gait / MGI
- limb grasping / MGI
- infertility / MGI
- male infertility / MGI
- female infertility / MGI
- abnormal limb morphology / MGI
- abnormal digit morphology / MGI
- no abnormal phenotype detected / MGI
- small uterus / MGI
- abnormal sperm motility / MGI
- short fibula / MGI
- abnormal uterus development / MGI
- abnormal oviduct morphology / MGI
- abnormal Mullerian duct morphology / MGI
- scapular bone foramen / MGI
- short humerus / MGI
- absent ulna / MGI
- abnormal ulna morphology / MGI
- abnormal humerus morphology / MGI
- hearing/vestibular/ear phenotype / MGI
- reproductive system phenotype / MGI
- skeleton phenotype / MGI
- vision/eye phenotype / MGI
- abnormal limb development / MGI
- thin myometrium / MGI
- fused phalanges / MGI
- hemimelia / MGI
- short oviduct / MGI
- thin uterus / MGI
- absent endometrial glands / MGI
- failure of Mullerian duct regression / MGI
- abnormal skin appearance / MGI
- prenatal lethality, incomplete penetrance / MGI
C57BL/6NCrl-Wnt7aem1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:14852 |
Citation information | RRID:IMSR_EM:14852 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 | C57BL/6NCrl-Wnt7aem1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Wnt7aem1(IMPC)Ccpcz |
Gene/Transgene symbol | Wnt7a |
Information from provider
Provider | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
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 | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Fuhrmann syndrome / Orphanet_2854
- Phocomelia, Schinzel type / Orphanet_2879
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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