- abnormal heart morphology / IMPC
- enlarged spleen / IMPC
- abnormal eye morphology / IMPC
- abnormal heart looping / IMPC
- microphthalmia / IMPC
- prenatal lethality prior to heart atrial septation / IMPC
- persistence of hyaloid vascular system / IMPC
- abnormal embryo turning / IMPC
- abnormal pharyngeal arch morphology / IMPC
- abnormal vitelline vasculature morphology / IMPC
- abnormal placenta morphology / IMPC
- abnormal visceral yolk sac morphology / IMPC
- abnormal spleen morphology / IMPC
- decreased locomotor activity / IMPC
- eye hemorrhage / IMPC
- abnormal optic vesicle formation / IMPC
- embryonic growth retardation / IMPC
- preweaning lethality, complete penetrance / IMPC
- abnormal neural tube morphology / IMPC
- abnormal somite shape / IMPC
C57BL/6J-Vcanem1H/H
Status | Available to order |
EMMA ID | EM:12536 |
Citation information | RRID:IMSR_EM:12536 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/6J-Vcanem1H/H |
Alternative name | VCAN-E441A-EM1-B6 |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Vcanem1H |
Gene/Transgene symbol | Vcan |
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. |
Phenotypic information | Homozygous:Not knownHeterozygous:None reported |
Breeding history | Co-isogenic on original background |
References | None available |
Homozygous fertile | yes |
Homozygous viable | not known |
Homozygous matings required | no |
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
- Wagner disease / Orphanet_898
IMPC phenotypes (gene matching)
Information on how we integrate external resources can be found here
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