- 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-Cxcr4em1(cre)H/H
Status | Available to order |
EMMA ID | EM:15130 |
International strain name | C57BL/6NTac-Cxcr4em1(cre)H/H |
Alternative name | Cxcr4-CRE-EM1-B6N |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Cxcr4em1(cre)H |
Gene/Transgene symbol | Cxcr4 |
Information from provider
Provider | MRC-Harwell |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
Breeding history | Co-isogenic on original 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)
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).