- abnormal heart morphology / IMPC
- enlarged heart / IMPC
- abnormal spleen morphology / IMPC
- abnormal skeletal muscle morphology / IMPC
- abnormal uterus morphology / IMPC
- abnormal skin morphology / IMPC
- abnormal eye morphology / IMPC
- abnormal digit morphology / IMPC
- abnormal kidney morphology / IMPC
- decreased lean body mass / IMPC
- decreased NK cell number / IMPC
- hydrometra / IMPC
- decreased effector memory T-helper cell number / IMPC
C57BL/6NCrl-Flt3em1(IMPC)Ccpcz/Ph
Status | Under development - register interest |
EMMA ID | EM:13110 |
International strain name | C57BL/6NCrl-Flt3em1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Flt3em1(IMPC)Ccpcz |
Gene/Transgene symbol | Flt3 |
Information from provider
Provider | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
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 | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Acute myeloblastic leukemia with maturation / Orphanet_98834
- Acute myeloid leukemia with minimal differentiation / Orphanet_98832
- Acute myeloblastic leukemia without maturation / Orphanet_98833
- Mixed phenotype acute leukemia / Orphanet_530995
- Precursor B-cell acute lymphoblastic leukemia / Orphanet_99860
- Precursor T-cell acute lymphoblastic leukemia / Orphanet_99861
- B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality / Orphanet_585877
- Mixed phenotype acute leukemia with t(v;11q23.3) / Orphanet_589595
- Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2) / Orphanet_589534
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- hydrometra / IMPC
- decreased lean body mass / IMPC
- abnormal kidney morphology / IMPC
- abnormal spleen morphology / IMPC
- decreased NK cell number / IMPC
- abnormal heart morphology / IMPC
- decreased effector memory T-helper cell number / IMPC
- abnormal eye morphology / IMPC
- abnormal skeletal muscle morphology / IMPC
- abnormal uterus morphology / IMPC
- enlarged heart / IMPC
- abnormal skin morphology / IMPC
- abnormal digit morphology / IMPC
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