B6NCrl;B6N-Atm1Brd Trpm6tm1a(KOMP)Wtsi/CipheOrl
Status | Available to order |
EMMA ID | EM:10341 |
Citation information | RRID:IMSR_EM:10341 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 | B6NCrl;B6N-Atm1Brd Trpm6tm1a(KOMP)Wtsi/CipheOrl |
Alternative name | EPD0741_2_G10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Trpm6tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Trpm6 |
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 | Centre d'ImmunoPhenomique - Ciphe |
Provider affiliation | Centre d |
Genetic information | This mouse line originates from KOMP ES clone EPD0741_2_G10. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Primary hypomagnesemia with secondary hypocalcemia / Orphanet_30924
IMPC phenotypes (gene matching)