B6Brd;B6N-Tyrc-Brd Rnaseh2btm1a(EUCOMM)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:05078 |
International strain name | B6Brd;B6N-Tyrc-Brd Rnaseh2btm1a(EUCOMM)Wtsi/WtsiCnbc |
Alternative name | EPD0087_4_A02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Rnaseh2btm1a(EUCOMM)Wtsi, |
Gene/Transgene symbol | Rnaseh2b |
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 mouse line originates from EUCOMM ES clone EPD0087_4_A02. 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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Aicardi-Goutières syndrome / Orphanet_51
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- decreased cell proliferation / MGI
- liver hypoplasia / MGI
- abnormal blood vessel morphology / MGI
- decreased embryo size / MGI
- edema / MGI
- thymus hypoplasia / MGI
- hemorrhage / MGI
- embryonic growth retardation / MGI
- decreased birth body size / MGI
- preweaning lethality / MGI
- perinatal lethality, complete penetrance / MGI
- decreased fibroblast proliferation / MGI
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