- 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 |
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 |
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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