C57BL/6NTac-Nmnat1tm1a(EUCOMM)Wtsi/Cnrm
Status | Available to order |
EMMA ID | EM:04346 |
Citation information | RRID:IMSR_EM:04346 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/6NTac-Nmnat1tm1a(EUCOMM)Wtsi/Cnrm |
Alternative name | EPD0060_1_C04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Nmnat1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Nmnat1 |
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 | CNR, Consiglio Nazionale delle Ricerche |
Provider affiliation | EMMA-Monterotondo Campus International Development, CNR, Consiglio Nazionale delle Ricerche |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0060_1_C04. 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 | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Animals used for archiving | heterozygous C57BL/6NTac males, wild-type C57BL/6NTac females |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Cone rod dystrophy / Orphanet_1872
- Leber congenital amaurosis / Orphanet_65
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal retina morphology / MGI
- retinal degeneration / MGI
- abnormal retinal vasculature morphology / MGI
- no phenotypic analysis / MGI
- nervous system phenotype / MGI
- abnormal retinal inner nuclear layer morphology / MGI
- abnormal rod electrophysiology / MGI
- abnormal cone electrophysiology / MGI
- growth/size/body region phenotype / MGI
- behavior/neurological phenotype / MGI
- reproductive system phenotype / MGI
- retinal pigment epithelium atrophy / MGI
- impaired pupillary reflex / MGI
- retinal photoreceptor degeneration / MGI
- thin retinal inner nuclear layer / MGI
- disorganized retinal inner nuclear layer / MGI
- thin retinal outer nuclear layer / MGI
- retinal outer nuclear layer degeneration / MGI
- photoreceptor inner segment degeneration / MGI
- photoreceptor outer segment degeneration / MGI
- mortality/aging / MGI
- prenatal lethality, complete penetrance / MGI
- decreased total retina thickness / MGI
- decreased a wave amplitude / MGI
- decreased b wave amplitude / MGI
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