C57BL/6N-Prph2tm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:04943 |
International strain name | C57BL/6N-Prph2tm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0549_4_F09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Prph2tm1a(EUCOMM)Hmgu, |
Gene/Transgene symbol | Prph2 |
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 HEPD0549_4_F09. 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
- Adult-onset foveomacular vitelliform dystrophy / Orphanet_99000
- Butterfly-shaped pigment dystrophy / Orphanet_99001
- Cone rod dystrophy / Orphanet_1872
- Retinitis punctata albescens / Orphanet_52427
- Retinitis pigmentosa / Orphanet_791
- Multifocal pattern dystrophy simulating fundus flavimaculatus / Orphanet_99003
- Central areolar choroidal dystrophy / Orphanet_75377
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