- 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 |
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, wild-type FVB/N |
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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