B6Dnk;B6N-Cul7tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:04404 |
International strain name | B6Dnk;B6N-Cul7tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0069_3_A11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cul7tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Cul7 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0069_3_A11. 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 |
Animals used for archiving | heterozygous C57BL/6Dnk |
Breeding at archiving centre | Chimeras were mated to C57BL/6N Tac Den and maintained on this background thereafter. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- 3M syndrome / Orphanet_2616
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal vascular development / MGI
- decreased embryo size / MGI
- abnormal placenta development / MGI
- decreased trophoblast giant cell number / MGI
- hemorrhage / MGI
- respiratory distress / MGI
- no phenotypic analysis / MGI
- fetal growth retardation / MGI
- early cellular replicative senescence / MGI
- neonatal lethality, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
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