- vertebral fusion / IMPC
C57BL/6N-Atm1Brd Abca4tm1a(EUCOMM)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:05898 |
Citation information | RRID:IMSR_EM:05898 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-Atm1Brd Abca4tm1a(EUCOMM)Wtsi/WtsiIeg |
Alternative name | EPD0480_3_A06 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Abca4tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Abca4 |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0480_3_A06. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Cone rod dystrophy / Orphanet_1872
- Stargardt disease / Orphanet_827
- Retinitis pigmentosa / Orphanet_791
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- vertebral fusion / IMPC
MGI phenotypes (allele matching)
- increased mean corpuscular hemoglobin / MGI
MGI phenotypes (gene matching)
- delayed dark adaptation / MGI
- abnormal photoreceptor outer segment morphology / MGI
- abnormal retinal pigment epithelium morphology / MGI
- abnormal Bruch membrane morphology / MGI
- abnormal eye physiology / MGI
- vision/eye phenotype / MGI
- increased mean corpuscular hemoglobin / MGI
- retinal photoreceptor degeneration / MGI
- thin retinal outer nuclear layer / MGI
- photoreceptor outer segment degeneration / MGI
- lipofuscinosis / MGI
- abnormal vitamin A level / MGI
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