C57BL/6NTac-Cir1tm3a(KOMP)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:11497 |
Citation information | RRID:IMSR_EM:11497 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-Cir1tm3a(KOMP)Wtsi/WtsiIeg |
Alternative name | BEPD0009_1_E01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cir1tm3a(KOMP)Wtsi |
Gene/Transgene symbol | Cir1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone BEPD0009_1_E01. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Disease and phenotype information
IMPC phenotypes (allele matching)
MGI phenotypes (allele matching)
- absent vertebral pedicles / MGI
- rib bifurcation / MGI
- rib fusion / MGI
- scoliosis / MGI
- overriding aortic valve / MGI
- abnormal atrioventricular cushion morphology / MGI
- abnormal large intestine morphology / MGI
- abnormal ureter morphology / MGI
- abnormal thyroid gland morphology / MGI
- abnormal forebrain morphology / MGI
- small kidney / MGI
- decreased rib number / MGI
- abnormal eye muscle morphology / MGI
- abnormal Mullerian duct morphology / MGI
- abnormal Wolffian duct morphology / MGI
- abnormal optic cup morphology / MGI
- occipital bone foramen / MGI
- fusion of vertebral arches / MGI
- decreased cervical vertebrae number / MGI
- perimembraneous ventricular septal defect / MGI
- abnormal pulmonary valve cusp morphology / MGI
- abnormal hypoglossal nerve topology / MGI
- subcutaneous edema / MGI
- absent costovertebral joint / MGI
- absent intracranial segment of vertebral artery / MGI
- multiple persisting craniopharyngeal ducts / MGI
- additional anastomosis between intracranial vertebral arteries / MGI
- heterochrony / MGI
MGI phenotypes (gene matching)
- absent vertebral pedicles / MGI
- rib bifurcation / MGI
- rib fusion / MGI
- scoliosis / MGI
- overriding aortic valve / MGI
- abnormal atrioventricular cushion morphology / MGI
- abnormal large intestine morphology / MGI
- abnormal ureter morphology / MGI
- abnormal thyroid gland morphology / MGI
- abnormal forebrain morphology / MGI
- small kidney / MGI
- decreased rib number / MGI
- abnormal eye muscle morphology / MGI
- abnormal Mullerian duct morphology / MGI
- abnormal Wolffian duct morphology / MGI
- abnormal optic cup morphology / MGI
- occipital bone foramen / MGI
- fusion of vertebral arches / MGI
- decreased cervical vertebrae number / MGI
- perimembraneous ventricular septal defect / MGI
- abnormal pulmonary valve cusp morphology / MGI
- abnormal hypoglossal nerve topology / MGI
- subcutaneous edema / MGI
- absent costovertebral joint / MGI
- absent intracranial segment of vertebral artery / MGI
- multiple persisting craniopharyngeal ducts / MGI
- additional anastomosis between intracranial vertebral arteries / MGI
- heterochrony / MGI
- persistent trigeminal artery / MGI
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