- abnormal blood vessel morphology / IMPC
- microphthalmia / IMPC
- increased lymphocyte cell number / IMPC
- abnormal placenta morphology / IMPC
- abnormal kidney morphology / IMPC
- abnormal limb morphology / IMPC
- increased leukocyte cell number / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal skin morphology / IMPC
- embryonic growth retardation / IMPC
- enlarged spleen / IMPC
- increased monocyte cell number / IMPC
- abnormal placenta size / IMPC
- abnormal eyelid morphology / IMPC
- cataract / IMPC
- enlarged testis / IMPC
- enlarged kidney / IMPC
- abnormal testis morphology / IMPC
- abnormal vitreous body morphology / IMPC
- abnormal spleen morphology / IMPC
- persistence of hyaloid vascular system / IMPC
- decreased circulating creatinine level / IMPC
- edema / IMPC
C57BL/6NTac-Cxcr4em2H/H
Status | Available to order |
EMMA ID | EM:15585 |
Citation information | RRID:IMSR_EM:15585 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-Cxcr4em2H/H |
Alternative name | C57BL/6NTac-Cxcr4em2H/H |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Cxcr4em2H |
Gene/Transgene symbol | Cxcr4 |
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | As reported by Mouse Genome Informatics, Cxcr4, a protein coding gene, codes for C-X-C chemokine receptor 4 and is associated with WHIM syndrome, cardiomyopathy and congestive heart failure in both mice and humans. ERT2 cassette knock-in to the existing Cxcr4-CRE-EM1-B6N allele, made by CRISPR/Cas9 gene editing via pronuclear injection of reagents into 1-cell stage embryo. |
Phenotypic information | Homozygous:To be confirmedHeterozygous:To be confirmed |
Breeding history | Incepient congenic on maintained background |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
Immunocompromised | not known |
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
- WHIM syndrome / Orphanet_51636
IMPC phenotypes (gene matching)
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