C57BL/6N-Atm1Brd Tmem126atm1a(EUCOMM)Wtsi/WtsiCnrm
Status | Available to order |
EMMA ID | EM:08260 |
Citation information | RRID:IMSR_EM:08260 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 Tmem126atm1a(EUCOMM)Wtsi/WtsiCnrm |
Alternative name | EPD0409_3_A09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Tmem126atm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Tmem126a |
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 EPD0409_3_A09. 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 |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive optic atrophy, OPA7 type / Orphanet_227976
IMPC phenotypes (allele matching)
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