- abnormal tooth development / MGI
- impaired coordination / MGI
- absent mesoderm / MGI
- failure to gastrulate / MGI
- abnormal dorsal-ventral axis patterning / MGI
- abnormal placenta morphology / MGI
- increased thermal nociceptive threshold / MGI
- neoplasm / MGI
- increased malignant tumor incidence / MGI
- increased lung adenocarcinoma incidence / MGI
- increased neurofibrosarcoma incidence / MGI
- increased sarcoma incidence / MGI
- increased carcinoma incidence / MGI
- abnormal developmental patterning / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal extraembryonic tissue morphology / MGI
- disorganized extraembryonic tissue / MGI
- absent extraembryonic ectoderm / MGI
- small ectoplacental cone / MGI
- abnormal renal tubule morphology / MGI
- nervous system phenotype / MGI
- increased osteosarcoma incidence / MGI
- abnormal osteoblast morphology / MGI
- abnormal action potential / MGI
- abnormal axon morphology / MGI
- increased mesothelioma incidence / MGI
- increased osteoma incidence / MGI
- increased neurofibroma incidence / MGI
- osseous metaplasia / MGI
- increased fibrosarcoma incidence / MGI
- increased fibroadenoma incidence / MGI
- increased renal carcinoma incidence / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality between implantation and somite formation, incomplete penetrance / MGI
- abnormal visceral endoderm morphology / MGI
- increased lymphoma incidence / MGI
FVB;129P2-Nf2tm2Gth/Cnrm
Status | Available to order |
EMMA ID | EM:00408 |
Citation information | RRID:IMSR_EM:00408 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 | FVB;129P2-Nf2tm2Gth/Cnrm |
Alternative name | Nf2F |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Nf2tm2Gth |
Gene/Transgene symbol | Nf2 |
Information from provider
Provider | Anton Berns |
Provider affiliation | Research - Animal Facility, The Netherlands Cancer Institute |
Genetic information | Insertion of loxP sequences into intron 2 and 3. |
Phenotypic information | Conditional Nf2 knock-out, no phenotype. |
References |
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Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Animals used for archiving | heterozygous FVB/N males, wild-type FVB/N females |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Meningioma / Orphanet_2495
- Neurofibromatosis type 2 / Orphanet_637
MGI phenotypes (gene matching)
Literature references
- Conditional biallelic Nf2 mutation in the mouse promotes manifestations of human neurofibromatosis type 2.;Giovannini M, Robanus-Maandag E, van der Valk M, Niwa-Kawakita M, Abramowski V, Goutebroze L, Woodruff J M, Berns A, Thomas G, ;2000;Genes & development;14;1617-30; 10887156
Information on how we integrate external resources can be found here
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