- decreased circulating fructosamine level / IMPC
- hyperplasia / IMPC
- increased heart weight / IMPC
- extramedullary hemopoiesis / IMPC
- increased circulating magnesium level / IMPC
- decreased circulating HDL cholesterol level / IMPC
- decreased circulating cholesterol level / IMPC
- increased circulating calcium level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- decreased circulating creatinine level / IMPC
- increased circulating amylase level / IMPC
B6Brd;B6N-Tyrc-Brd-Slc16a2tm1c(KOMP)Wtsi/WtsiCnrm
Status | Available to order |
EMMA ID | EM:13413 |
Citation information | RRID:IMSR_EM:13413 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 | B6Brd;B6N-Tyrc-Brd-Slc16a2tm1c(KOMP)Wtsi/WtsiCnrm |
Alternative name | EPD0109_3_E07 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Slc16a2tm1c(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 conditional allele tm1c. 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
- Allan-Herndon-Dudley syndrome / Orphanet_59
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased circulating LDL cholesterol level / MGI
- decreased circulating HDL cholesterol level / MGI
- increased circulating alkaline phosphatase level / MGI
- nervous system phenotype / MGI
- decreased circulating cholesterol level / MGI
- abnormal circulating hormone level / MGI
- abnormal thyroxine level / MGI
- abnormal triiodothyronine level / MGI
- increased triiodothyronine level / MGI
- decreased circulating thyroxine level / MGI
- increased circulating triiodothyronine level / MGI
- decreased circulating creatinine level / MGI
- increased circulating amylase level / MGI
- decreased circulating fructosamine level / MGI
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