- increased mean corpuscular hemoglobin / MGI
C57BL/6NTac-Eif2b2tm2a(KOMP)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:14107 |
Citation information | RRID:IMSR_EM:14107 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 | C57BL/6NTac-Eif2b2tm2a(KOMP)Wtsi/WtsiH |
Alternative name | EPD0168_1_D04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Eif2b2tm2a(KOMP)Wtsi |
Gene/Transgene symbol | Eif2b2 |
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 KOMP ES clone EPD0168_1_D04. 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
- Congenital or early infantile CACH syndrome / Orphanet_157713
- Late infantile CACH syndrome / Orphanet_157716
- Ovarioleukodystrophy / Orphanet_99853
- Juvenile or adult CACH syndrome / Orphanet_157719
- Cree leukoencephalopathy / Orphanet_99854
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- increased mean corpuscular hemoglobin / MGI
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