C57BL/6N-Mgat1tm1a(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:08518 |
International strain name | C57BL/6N-Mgat1tm1a(EUCOMM)Hmgu/Ieg |
Alternative name | HEPD0661_3_D04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Mgat1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Mgat1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0661_3_D04. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTac |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal vascular development / MGI
- abnormal embryonic neuroepithelial layer differentiation / MGI
- incomplete rostral neuropore closure / MGI
- anemia / MGI
- incomplete somite formation / MGI
- decreased embryo size / MGI
- incomplete embryo turning / MGI
- abnormal left-right axis patterning / MGI
- embryonic growth arrest / MGI
- hemorrhage / MGI
- abnormal neural tube morphology / MGI
- situs inversus / MGI
- pallor / MGI
- embryonic growth retardation / MGI
- abnormal direction of heart looping / MGI
- abnormal vascular endothelial cell morphology / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- incomplete caudal neuropore closure / MGI
- abnormal tail position or orientation / MGI
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