- abnormal retinal photoreceptor morphology / MGI
- abnormal retinal cone cell morphology / MGI
- abnormal eye development / MGI
- abnormal retina morphology / MGI
- retinal degeneration / MGI
- abnormal macrophage morphology / MGI
- abnormal retinal vasculature morphology / MGI
- abnormal retinal layer morphology / MGI
- abnormal retinal photoreceptor layer morphology / MGI
- abnormal photoreceptor outer segment morphology / MGI
- abnormal photoreceptor inner segment morphology / MGI
- abnormal retinal outer nuclear layer morphology / MGI
- abnormal retinal outer plexiform layer morphology / MGI
- abnormal rod electrophysiology / MGI
- abnormal cone electrophysiology / MGI
- abnormal retinal pigment epithelium morphology / MGI
- abnormal Muller cell morphology / MGI
- abnormal eye electrophysiology / MGI
- abnormal retinal neuronal layer morphology / MGI
- increased retinal cone cell number / MGI
- absent retinal cone cells / MGI
- decreased retinal rod cell number / MGI
- absent retinal rod cells / MGI
- abnormal retinal rod cell outer segment morphology / MGI
- thin retinal outer nuclear layer / MGI
- disorganized retinal outer nuclear layer / MGI
- retinal outer nuclear layer degeneration / MGI
- thin retinal outer plexiform layer / MGI
- absent photoreceptor outer segment / MGI
- disorganized photoreceptor outer segment / MGI
- short photoreceptor outer segment / MGI
- retinal neovascularization / MGI
- abnormal retinal development / MGI
- decreased total retina thickness / MGI
- retinal spots / MGI
- increased retinal apoptosis / MGI
C57BL/6N-Prph2tm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:04943 |
Citation information | RRID:IMSR_EM:04943 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-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 | 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 males |
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
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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