C57BL/6N-Slc6a2tm1b(EUCOMM)Hmgu/Cnrm
Status | Available to order |
EMMA ID | EM:09028 |
International strain name | C57BL/6N-Slc6a2tm1b(EUCOMM)Hmgu/Cnrm |
Alternative name | HEPD0649_1_F02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Slc6a2tm1b(EUCOMM)Hmgu, |
Gene/Transgene symbol | Slc6a2 |
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 HEPD0649_1_F02. For further details on the construction of this clone see the page at the IMPC portal. The critical exon(s) were flanked by loxP sites, and subsequent cre expression excised this critical sequence resulting in a knockout reporter allele (Gt(ROSA)26Sortm1(ACTB-cre,-EGFP)Ics (MGI:5285392)). Click here for more information on EUCOMM final vectors. |
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
- Postural orthostatic tachycardia syndrome due to NET deficiency / Orphanet_443236
IMPC phenotypes (allele matching)
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