C57BL/6N-Rpe65tm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:04900 |
International strain name | C57BL/6N-Rpe65tm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0553_2_C10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Rpe65tm1a(EUCOMM)Hmgu, |
Gene/Transgene symbol | Rpe65 |
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 | Mammalian Genetics Unit, Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0553_2_C10. 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/6NTac |
Breeding at archiving centre | Chimeras were mated to C57BL/6N Tac USA, and maintained on this background thereafter. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Leber congenital amaurosis / Orphanet_65
- Retinitis pigmentosa / Orphanet_791
- Severe early-childhood-onset retinal dystrophy / Orphanet_364055
IMPC phenotypes (allele matching)
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