C57BL/6NTac-Pex16tm1a(EUCOMM)Hmgu/IcsOrl
Status | Available to order |
EMMA ID | EM:07735 |
Citation information | RRID:IMSR_EM:07735 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-Pex16tm1a(EUCOMM)Hmgu/IcsOrl |
Alternative name | HEPD0537_2_B03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Pex16tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Pex16 |
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 | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0537_2_B03. For further details on the construction of this clone see the page at the IKMC portal. Removal of the targeting cassette using Flp recombinase is required to convert the targeted into a conditional allele - more information on conversion to the b,c and d allele forms. Click here for more information on EUCOMM final vectors |
Phenotypic information | Potential EUMODIC data in the Europhenome database |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Zellweger syndrome / Orphanet_912
- Neonatal adrenoleukodystrophy / Orphanet_44
- Infantile Refsum disease / Orphanet_772
IMPC phenotypes (allele matching)
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