- abnormal vertebrae morphology / MGI
- abnormal rib morphology / MGI
- rib bifurcation / MGI
- rib fusion / MGI
- kinked tail / MGI
- short tail / MGI
- fused dorsal root ganglion / MGI
- abnormal female reproductive system morphology / MGI
- abnormal oocyte morphology / MGI
- small ovary / MGI
- impaired ovarian folliculogenesis / MGI
- abnormal ovarian folliculogenesis / MGI
- abnormal ovarian follicle morphology / MGI
- abnormal lung development / MGI
- decreased body length / MGI
- decreased caudal vertebrae number / MGI
- abnormal embryo development / MGI
- abnormal somite development / MGI
- reduced fertility / MGI
- male infertility / MGI
- female infertility / MGI
- abnormal gametogenesis / MGI
- postnatal lethality / MGI
- abnormal axial skeleton morphology / MGI
- abnormal pulmonary alveolus morphology / MGI
- abnormal retinal vasculature morphology / MGI
- abnormal rib development / MGI
- no phenotypic analysis / MGI
- abnormal thoracic vertebrae morphology / MGI
- abnormal lumbar vertebrae morphology / MGI
- abnormal sacral vertebrae morphology / MGI
- decreased rib number / MGI
- abnormal embryonic hematopoiesis / MGI
- abnormal lung vasculature morphology / MGI
- caudal body truncation / MGI
- vertebral fusion / MGI
- abnormal thoracic cage morphology / MGI
- decreased cervical vertebrae number / MGI
- absent caudal vertebrae / MGI
- abnormal female meiosis / MGI
- abnormal rostral-caudal axis patterning / MGI
- abnormal somite size / MGI
- abnormal dorsal-ventral polarity of the somites / MGI
- abnormal vertebrae development / MGI
- abnormal vertebral body development / MGI
- hearing/vestibular/ear phenotype / MGI
- embryo phenotype / MGI
- skeleton phenotype / MGI
- impaired lung alveolus development / MGI
- abnormal sclerotome morphology / MGI
- abnormal sternocostal joint morphology / MGI
- abnormal costovertebral joint morphology / MGI
- abnormal rostral-caudal patterning of the somites / MGI
- decreased survivor rate / MGI
- mortality/aging / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- embryonic lethality, incomplete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
C57BL/6N-Lfngem1(IMPC)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:14574 |
Citation information | RRID:IMSR_EM:14574 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/6N-Lfngem1(IMPC)Wtsi/WtsiCnbc |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Lfngem1(IMPC)Wtsi |
Gene/Transgene symbol | Lfng |
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 males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive spondylocostal dysostosis / Orphanet_2311
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).