- vertebral fusion / IMPC
C57BL/6N-Atm1Brd Abca4tm1a(EUCOMM)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:05898 |
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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