- abnormal digestive system morphology / MGI
- right pulmonary isomerism / MGI
- abnormal liver morphology / MGI
- dextrocardia / MGI
- abnormal spleen morphology / MGI
- abnormal left-right axis patterning / MGI
- abnormal kidney morphology / MGI
- situs inversus / MGI
- transposition of great arteries / MGI
- heterotaxia / MGI
- abnormal vena cava morphology / MGI
- annular pancreas / MGI
- ventricular septal defect / MGI
- atrial septal defect / MGI
- complete atrioventricular septal defect / MGI
- neonatal lethality, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- lethality throughout fetal growth and development, incomplete penetrance / MGI
B6.129X1-Gdf1tm1Dmus/Kctt
| Status | Available to order |
| EMMA ID | EM:02230 |
| Citation information | RRID:IMSR_EM:02230 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 | B6.129X1-Gdf1tm1Dmus/Kctt |
| Alternative name | Gdf1-flox |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Gdf1tm1Dmus |
| Gene/Transgene symbol | Gdf1 |
Information from provider
| Provider | Ted Ebendal |
| Provider affiliation | Department of Neuroscience, Uppsala University |
| Genetic information | LoxP sites were introduced in introns flanking exon 2. The Neo cassette (flanked by frt sites) was eliminated in vivo by crossing with FLP deleters. |
| Phenotypic information | Mice carrying the Gdf1 floxed allele appear normal (also homozygotes). The floxed allele can be eliminated by crossing with a Cre deleter and result in many pups with situs inversus as described from the original Gdf1 knockout. We have eliminated Gdf1 in various nerve cells in the mouse (by cell specific Cre expression) and have seen only small effects. |
| References |
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Information from EMMA
| Archiving centre | Karolinska Institutet, Stockholm, Sweden |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Right sided atrial isomerism / Orphanet_97548
MGI phenotypes (gene matching)
Literature references
- Generation and characterization of a Gdf1 conditional null allele.;Bengtsson Henrik, Epifantseva Irina, Abrink Magnus, Kylberg Annika, Kullander Klas, Ebendal Ted, Usoskin Dmitry, ;2008;Genesis (New York, N.Y. : 2000);46;368-72; 18615710
- Growth/differentiation factor 1 alleviates pressure overload-induced cardiac hypertrophy and dysfunction.;Zhang Yan, Zhang Xiao-Fei, Gao Lu, Liu Yu, Jiang Ding-Sheng, Chen Ke, Yang Qinglin, Fan Guo-Chang, Zhang Xiao-Dong, Huang Congxin, ;2014;Biochimica et biophysica acta;1842;232-44; 24275554
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