- hyperactivity / IMPC
- decreased locomotor activity / IMPC
- decreased vertical activity / IMPC
- decreased exploration in new environment / IMPC
- decreased lean body mass / IMPC
- increased total body fat amount / IMPC
- increased hematocrit / IMPC
- decreased food intake / IMPC
- decreased respiratory quotient / IMPC
- decreased bone mineral content / IMPC
- abnormal seminal vesicle morphology / IMPC
C57BL/6J-Del(7)57H/H
| Status | Available to order |
| EMMA ID | EM:16973 |
| Citation information | RRID:IMSR_EM:16973 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 | C57BL/6J-Del(7)57H/H |
| Alternative name | C57BL/6J-Del(7)57H/H |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Del(7)57H |
| Gene/Transgene symbol | Ube3a |
Information from provider
| Provider | Theresa Strong |
| Provider affiliation | |
| Genetic information | This strain carries a Deletion of 3,089,372 nt from Chromosome 7. The strain was generated by CRISPR/Cas9 induced deletion of 3 mega base pairs from 7:59336000-59337600 (between Ube3a and snoRNAs) and 7:62423586-62427187 (between Mkm3 and Peg12). This region is imprinted, it should be maintained through the female line for breeding and through the male line when producing experimental animals. |
| Phenotypic information | Homozygous:not determinedHeterozygous:perinatal lethal when inherited paternally. |
| Breeding history | Coisogenic on C57BL/6J |
| References | None available |
| Homozygous fertile | no |
| Homozygous viable | no |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Angelman syndrome due to a point mutation / Orphanet_411511
IMPC phenotypes (gene matching)
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