FVB.129P2-Csf3rtm2Eur/Cnrm
Status | Available to order |
EMMA ID | EM:00054 |
Citation information | RRID:IMSR_EM:00054 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 | FVB.129P2-Csf3rtm2Eur/Cnrm |
Alternative name | Csfgr-KO |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Csf3rtm2Eur |
Gene/Transgene symbol | Csf3r |
Information from provider
Provider | Mirjam Hermans |
Provider affiliation | Erasmus Univ.-Inst. Hematology |
Genetic information | Inactivation of the Csf3r (Csfgr, G-CSFR) gene. Exons 7 to 17 are replaced by a PGK-neo gene (the total number of exons in the Csf3r gene is 17). |
Phenotypic information | Reduced numbers of bone marrow and blood neutrophils. |
References | None available |
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Chronic neutrophilic leukemia / Orphanet_86829
- Atypical chronic myeloid leukemia / Orphanet_98824
- Autosomal recessive severe congenital neutropenia due to CSF3R deficiency / Orphanet_420702
- Hereditary neutrophilia / Orphanet_279943
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- decreased neutrophil cell number / MGI
MGI phenotypes (gene matching)
- decreased neutrophil cell number / MGI
- decreased monocyte cell number / MGI
- increased bone marrow cell number / MGI
- decreased bone marrow cell number / MGI
- decreased granulocyte number / MGI
- abnormal hematopoietic system morphology/development / MGI
- abnormal bone marrow cell morphology/development / MGI
- abnormal myeloblast morphology/development / MGI
- abnormal neutrophil differentiation / MGI
- abnormal neutrophil physiology / MGI
- abnormal monocyte morphology / MGI
- decreased hematopoietic stem cell number / MGI
- immune system phenotype / MGI
- abnormal common myeloid progenitor cell morphology / MGI
- impaired neutrophil chemotaxis / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).