C57BL/6NTac-Gfi1btm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:06985 |
Citation information | RRID:IMSR_EM:06985 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-Gfi1btm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0515_4_E11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Gfi1btm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Gfi1b |
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 HEPD0515_4_E11. 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
- Gray platelet syndrome / Orphanet_721
- Autosomal dominant macrothrombocytopenia / Orphanet_140957
- Alpha delta granule deficiency / Orphanet_734
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- absent erythrocytes / MGI
- abnormal megakaryocyte differentiation / MGI
- abnormal erythropoiesis / MGI
- internal hemorrhage / MGI
- edema / MGI
- hemorrhage / MGI
- pallor / MGI
- abnormal embryonic erythropoiesis / MGI
- abnormal embryonic erythrocyte morphology / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
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