- thin ventricular wall / MGI
- abnormal myelination / MGI
- abnormal Schwann cell morphology / MGI
- decreased body size / MGI
- impaired limb coordination / MGI
- internal hemorrhage / MGI
- postnatal growth retardation / MGI
- edema / MGI
- pericardial edema / MGI
- abnormal blood circulation / MGI
- abnormal myocardial trabeculae morphology / MGI
- abnormal sciatic nerve morphology / MGI
- thin myocardium / MGI
- akinesia / MGI
- abnormal somatic nervous system morphology / MGI
- abnormal endocardium morphology / MGI
- abnormal cochlear nerve morphology / MGI
- increased triglyceride level / MGI
- cardiovascular system phenotype / MGI
- abnormal axon morphology / MGI
- abnormal mitochondrion morphology / MGI
- dilated heart ventricle / MGI
- abnormal fetal cardiomyocyte morphology / MGI
- abnormal axon fasciculation / MGI
- myocardial trabeculae hypoplasia / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- preweaning lethality, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- abnormal mitochondrial shape / MGI
- abnormal mitochondrial crista morphology / MGI
- abnormal axon radial sorting / MGI
- joint contracture / MGI
C3HeB/FeJ-Adgrg6m1Mhda/Ieg
| Status | Available to order |
| EMMA ID | EM:09067 |
| Citation information | RRID:IMSR_EM:09067 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 | C3HeB/FeJ-Adgrg6m1Mhda/Ieg |
| Alternative name | Gpr126H7622YMhda |
| Strain type | Induced Mutant Strains : Chemically-induced |
| Allele/Transgene symbol | Adgrg6m1Mhda |
| Gene/Transgene symbol | Adgrg6 |
Information from provider
| Provider | Martin Hrabe de Angelis |
| Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum München |
| Genetic information | 2284C->T point mutation of Gpr126. |
| Phenotypic information | Homozygous:Homozygous mice viable, no obvious phenotype observed.Heterozygous:No obvious phenotype observed. |
| References | None available |
| Homozygous fertile | yes |
| Homozygous viable | yes |
| 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 C3H males |
Disease and phenotype information
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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