C57BL/6NTac-Cir1tm3a(KOMP)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:11497 |
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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