- abnormal cell physiology / MGI
- abnormal embryo development / MGI
- decreased embryo size / MGI
- abnormal visceral yolk sac morphology / MGI
- absent vitelline blood vessels / MGI
- abnormal extraembryonic tissue morphology / MGI
- abnormal pluripotent precursor cell morphology / MGI
- abnormal embryonic-extraembryonic boundary morphology / MGI
- embryonic growth retardation / MGI
- enlarged allantois / MGI
- absent somites / MGI
- absent chorion / MGI
- embryonic lethality between somite formation and embryo turning, complete penetrance / MGI
- decreased inner cell mass proliferation / MGI
B6.129S2-Hsd17b12Gt(A030E06)Wrst/Ieg
| Status | Available to order |
| EMMA ID | EM:05695 |
| Citation information | RRID:IMSR_EM:05695 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-Hsd17b12Gt(A030E06)Wrst/Ieg |
| Alternative name | Hsd17b12 (hydroxysteroid (17-beta) dehydrogenase 12) |
| Strain type | Gene-trap |
| Allele/Transgene symbol | Hsd17b12Gt(A030E06)Wrst |
| Gene/Transgene symbol | Hsd17b12 |
Information from provider
| Provider | Franz Vauti |
| Provider affiliation | Cell- & Molecular Biology, Technical University of Braunschweig |
| Genetic information | Hsd17b12 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
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal embryo development / MGI
- decreased embryo size / MGI
- abnormal visceral yolk sac morphology / MGI
- absent vitelline blood vessels / MGI
- abnormal extraembryonic tissue morphology / MGI
- abnormal pluripotent precursor cell morphology / MGI
- abnormal embryonic-extraembryonic boundary morphology / MGI
- embryonic growth retardation / MGI
- enlarged allantois / MGI
- abnormal cell physiology / MGI
- absent somites / MGI
- absent chorion / MGI
- embryonic lethality between somite formation and embryo turning, complete penetrance / MGI
- decreased inner cell mass proliferation / 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
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).
