B6Brd;B6Dnk;B6N-Tyrc-Brd-Slc16a2tm1d(KOMP)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:10802 |
International strain name | B6Brd;B6Dnk;B6N-Tyrc-Brd-Slc16a2tm1d(KOMP)Wtsi/WtsiH |
Alternative name | EPD0109_3_E07 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Slc16a2tm1d(KOMP)Wtsi |
Gene/Transgene symbol | Slc16a2 |
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 line originates from KOMP ES clone EPD0109_3_E07, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a deletion allele tm1d (post-Flp and Cre with no reporter). 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Allan-Herndon-Dudley syndrome / Orphanet_59
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