- increased mean corpuscular hemoglobin / MGI
C57BL/6NTac-Eif2b2tm2a(KOMP)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:14107 |
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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