- decreased thigmotaxis / IMPC
- decreased locomotor activity / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal behavior / IMPC
- enlarged lymph nodes / IMPC
- dysplasia / IMPC
- abnormal retina morphology / IMPC
- abnormal skin morphology / IMPC
- decreased anxiety-related response / IMPC
- abnormal lymph node morphology / IMPC
B6.129S2-Fubp1Gt(A033A08)Wrst/VauIeg
| Status | Available to order |
| EMMA ID | EM:05684 |
| Citation information | RRID:IMSR_EM:05684 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 | B6.129S2-Fubp1Gt(A033A08)Wrst/VauIeg |
| Alternative name | Fubp1 (far upstream element (FUSE) binding protein 1) |
| Strain type | Gene-trap |
| Allele/Transgene symbol | Fubp1Gt(A033A08)Wrst |
| Gene/Transgene symbol | Fubp1 |
Information from provider
| Provider | Franz Vauti |
| Provider affiliation | Cell- & Molecular Biology, Technical University of Braunschweig |
| Genetic information | Fubp1 Gt PT1betageo. |
| Phenotypic information | Not known; mouse line not yet characterized. |
| Breeding history | Backcrossed into C57BL/6 (N>7). |
| References |
|
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | not known |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
| Animals used for archiving | heterozygous C57BL/6J males |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased bone marrow cell number / MGI
- small liver / MGI
- pale liver / MGI
- spleen hypoplasia / MGI
- abnormal stratification in cerebral cortex / MGI
- pulmonary hypoplasia / MGI
- anemia / MGI
- cardiac hypertrophy / MGI
- abnormal placenta morphology / MGI
- thymus hypoplasia / MGI
- hemorrhage / MGI
- abnormal definitive hematopoiesis / MGI
- abnormal blood circulation / MGI
- abnormal brain morphology / MGI
- lymphoid hypoplasia / MGI
- small lung / MGI
- pallor / MGI
- decreased fetal size / MGI
- decreased B cell number / MGI
- absent cerebellar lobules / MGI
- decreased megakaryocyte cell number / MGI
- abnormal cerebral hemisphere morphology / MGI
- abnormal hematopoietic stem cell physiology / MGI
- prenatal growth retardation / MGI
- abnormal prenatal body size / MGI
- abnormal pulmonary alveolar sac morphology / MGI
- impaired branching involved in alveolar sac morphogenesis / MGI
- neonatal lethality, complete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- thin placenta labyrinth / MGI
- abnormal placenta intervillous maternal lacunae morphology / MGI
- abnormal hematopoietic precursor cell number / MGI
Literature references
- A large-scale, gene-driven mutagenesis approach for the functional analysis of the mouse genome.;Hansen Jens, Floss Thomas, Van Sloun Petra, Füchtbauer Ernst-Martin, Vauti Franz, Arnold Hans-Hennig, Schnütgen Frank, Wurst Wolfgang, von Melchner Harald, Ruiz Patricia, ;2003;Proceedings of the National Academy of Sciences of the United States of America;100;9918-22; 12904583
- Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells.;Wiles M V, Vauti F, Otte J, Füchtbauer E M, Ruiz P, Füchtbauer A, Arnold H H, Lehrach H, Metz T, von Melchner H, Wurst W, ;2000;Nature genetics;24;13-4; 10615117
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