- abnormal cerebellum morphology / MGI
- Purkinje cell degeneration / MGI
- abnormal myelination / MGI
- hypoactivity / MGI
- abnormal brain morphology / MGI
- no abnormal phenotype detected / MGI
- neurodegeneration / MGI
- decreased vertical activity / MGI
- abnormal motor learning / MGI
- astrocytosis / MGI
- abnormal brain white matter morphology / MGI
- abnormal oligodendrocyte physiology / MGI
- microgliosis / MGI
- abnormal cerebellum white matter morphology / MGI
- increased oligodendrocyte number / MGI
C57BL/6N-Gjc2tm1b(EUCOMM)Wtsi/H
| Status | Only small colony available |
| EMMA ID | EM:16287 |
| Citation information | RRID:IMSR_EM:16287 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/6N-Gjc2tm1b(EUCOMM)Wtsi/H |
| Alternative name | EPD0803_2_A09 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Gjc2tm1b(EUCOMM)Wtsi |
| Gene/Transgene symbol | Gjc2 |
| 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 | Mary Lyon Centre at MRC Harwell |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from EUCOMM ES clone EPD0803_2_A09. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele. Click here for more information on EUCOMM final vectors. |
| 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
Orphanet associated rare diseases, based on orthologous gene matching
- Pelizaeus-Merzbacher-like disease due to GJC2 mutation / Orphanet_280282
- Autosomal recessive spastic paraplegia type 44 / Orphanet_320401
- Milroy disease / Orphanet_79452
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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