- 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 |
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
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).