- decreased bone mineral density / IMPC
- decreased hematocrit / IMPC
- abnormal cranium morphology / IMPC
- abnormal snout morphology / IMPC
- abnormal maxilla morphology / IMPC
- decreased body length / IMPC
- decreased body weight / IMPC
- abnormal tooth morphology / IMPC
- decreased hemoglobin content / IMPC
- decreased erythrocyte cell number / IMPC
- decreased lean body mass / IMPC
- decreased total body fat amount / IMPC
- decreased bone mineral content / IMPC
- hypoplasia / IMPC
- process of degenerative change / IMPC
- glomerulonephritis / IMPC
- lipid deposition / IMPC
- osteopenia / IMPC
- steatosis / IMPC
B6Brd;B6N-Tyrc-Brd Miga2tm1a(KOMP)Wtsi/WtsiH
| Status | Only small colony available |
| EMMA ID | EM:16564 |
| Citation information | RRID:IMSR_EM:16564 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 | B6Brd;B6N-Tyrc-Brd Miga2tm1a(KOMP)Wtsi/WtsiH |
| Alternative name | EPD0026_1_C12 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Miga2tm1a(KOMP)Wtsi |
| Gene/Transgene symbol | Miga2 |
| Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
| Provider | Wellcome Trust Sanger Institute |
| Provider affiliation | Wellcome Trust Sanger Institute |
| Genetic information | This mouse line originates from KOMP ES clone EPD0026_1_C12. For further details on the construction of this clone see the page at the IMPC portal. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased body weight / IMPC
- decreased lean body mass / IMPC
- process of degenerative change / IMPC
- hypoplasia / IMPC
- decreased erythrocyte cell number / IMPC
- decreased hematocrit / IMPC
- decreased bone mineral content / IMPC
- lipid deposition / IMPC
- decreased total body fat amount / IMPC
- osteopenia / IMPC
- abnormal cranium morphology / IMPC
- abnormal tooth morphology / IMPC
- steatosis / IMPC
- glomerulonephritis / IMPC
- abnormal snout morphology / IMPC
- abnormal maxilla morphology / IMPC
- decreased bone mineral density / IMPC
- decreased hemoglobin content / IMPC
- decreased body length / IMPC
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- decreased circulating LDL cholesterol level / MGI
- decreased circulating HDL cholesterol level / MGI
- decreased hematocrit / MGI
- abnormal cranium morphology / MGI
- abnormal snout morphology / MGI
- abnormal maxilla morphology / MGI
- decreased body length / MGI
- decreased body weight / MGI
- hyperactivity / MGI
- abnormal tooth morphology / MGI
- decreased hemoglobin content / MGI
- decreased lean body mass / MGI
- abnormal behavior / MGI
- decreased circulating cholesterol level / MGI
- decreased circulating serum albumin level / MGI
- decreased circulating total protein level / MGI
- decreased lactate dehydrogenase level / MGI
- decreased circulating aspartate transaminase level / MGI
- decreased total body fat amount / MGI
- decreased bone mineral content / MGI
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).
