C57BL/6NTac-Gfi1btm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:06985 |
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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