- abnormal coat/ hair morphology / IMPC
- abnormal forelimb morphology / IMPC
- abnormal hindlimb morphology / IMPC
- tremors / IMPC
- abnormal gait / IMPC
- decreased exploration in new environment / IMPC
- abnormal startle reflex / IMPC
- limb grasping / IMPC
- impaired righting response / IMPC
- increased mean platelet volume / IMPC
- increased circulating alkaline phosphatase level / IMPC
- increased circulating cholesterol level / IMPC
- improved glucose tolerance / IMPC
- increased circulating aspartate transaminase level / IMPC
- increased circulating creatinine level / IMPC
- decreased circulating glucose level / IMPC
- increased circulating iron level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
C57BL/6NTac-Tpoem1(IMPC)H/H
Status | Available to order |
EMMA ID | EM:12441 |
Citation information | RRID:IMSR_EM:12441 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-Tpoem1(IMPC)H/H |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Tpoem1(IMPC)H |
Gene/Transgene symbol | Tpo |
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project 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
- Hereditary isolated aplastic anemia / Orphanet_397692
- Familial thrombocytosis / Orphanet_71493
- Thrombocythemia with distal limb defects / Orphanet_329319
- Familial thyroid dyshormonogenesis / Orphanet_95716
- Congenital amegakaryocytic thrombocytopenia / Orphanet_3319
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- increased circulating aspartate transaminase level / IMPC
- decreased circulating glucose level / IMPC
- abnormal hindlimb morphology / IMPC
- abnormal startle reflex / IMPC
- abnormal coat/ hair morphology / IMPC
- impaired righting response / IMPC
- abnormal forelimb morphology / IMPC
- abnormal gait / IMPC
- tremors / IMPC
- increased mean platelet volume / IMPC
- increased circulating creatinine level / IMPC
- improved glucose tolerance / IMPC
- limb grasping / IMPC
- decreased exploration in new environment / IMPC
- increased circulating iron level / IMPC
- increased circulating cholesterol level / IMPC
- increased circulating alkaline phosphatase level / IMPC
- preweaning lethality, incomplete penetrance / IMPC
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