B6Dnk;B6N-Secisbp2tm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:04344 |
Citation information | RRID:IMSR_EM:04344 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 | B6Dnk;B6N-Secisbp2tm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0052_2_C03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Secisbp2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Secisbp2 |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0052_2_C03. 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 |
Animals used for archiving | heterozygous C57BL/6Dnk males |
Breeding at archiving centre | Chimeras were mated to C57BL/6Dnk and maintained on this background thereafter. |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Short stature-delayed bone age due to thyroid hormone metabolism deficiency / Orphanet_171706
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased circulating sodium level / IMPC
- abnormal retina morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- hyperplasia / IMPC
- increased leukocyte cell number / IMPC
- developmental and structural abnormality / IMPC
- decreased leukocyte cell number / IMPC
- increased NK cell number / IMPC
MGI phenotypes (allele matching)
- abnormal selenium level / MGI
- homeostasis/metabolism phenotype / MGI
- reproductive system phenotype / MGI
- embryonic growth arrest / MGI
- embryonic growth retardation / MGI
- preweaning lethality, complete penetrance / MGI
- embryonic lethality between implantation and placentation, incomplete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
MGI phenotypes (gene matching)
- embryonic growth arrest / MGI
- abnormal selenium level / MGI
- embryonic growth retardation / MGI
- homeostasis/metabolism phenotype / MGI
- reproductive system phenotype / MGI
- preweaning lethality, complete penetrance / MGI
- embryonic lethality between implantation and placentation, incomplete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
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