- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Atm1Brd Prrc2btm1a(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:05981 |
Citation information | RRID:IMSR_EM:05981 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/6N-Atm1Brd Prrc2btm1a(EUCOMM)Wtsi/WtsiBiat |
Alternative name | EPD0599_5_H02 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Prrc2btm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Prrc2b |
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 EUCOMM ES clone EPD0599_5_H02. 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 | University of Veterinary Medicine, Vienna, Austria |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- preweaning lethality, complete penetrance / IMPC
MGI phenotypes (allele matching)
- enlarged liver sinusoidal spaces / MGI
- abnormal thyroid gland morphology / MGI
- abnormal skeletal muscle morphology / MGI
- abnormal forebrain morphology / MGI
- hemorrhage / MGI
- abnormal eye morphology / MGI
- abnormal eye muscle morphology / MGI
- right aortic arch / MGI
- abnormal optic cup morphology / MGI
- fusion of vertebral arches / MGI
- absent skeletal muscle / MGI
- dilated vasculature / MGI
- arteriovenous malformation / MGI
- eye hemorrhage / MGI
- perimembraneous ventricular septal defect / MGI
- persistent right dorsal aorta / MGI
- abnormal pulmonary valve cusp morphology / MGI
- vacuolated lens / MGI
- absent hypoglossal canal / MGI
- absent hypoglossal nerve / MGI
- abnormal hypoglossal nerve topology / MGI
- absent segment of posterior cerebral artery / MGI
- retropleural edema / MGI
- persistent right 6th pharyngeal arch artery / MGI
- left sided brachiocephalic trunk / MGI
- abnormal vitelline vein topology / MGI
MGI phenotypes (gene matching)
- enlarged liver sinusoidal spaces / MGI
- abnormal thyroid gland morphology / MGI
- abnormal skeletal muscle morphology / MGI
- abnormal forebrain morphology / MGI
- hemorrhage / MGI
- abnormal eye morphology / MGI
- abnormal eye muscle morphology / MGI
- right aortic arch / MGI
- abnormal optic cup morphology / MGI
- fusion of vertebral arches / MGI
- absent skeletal muscle / MGI
- dilated vasculature / MGI
- arteriovenous malformation / MGI
- eye hemorrhage / MGI
- perimembraneous ventricular septal defect / MGI
- persistent right dorsal aorta / MGI
- abnormal pulmonary valve cusp morphology / MGI
- vacuolated lens / MGI
- absent hypoglossal canal / MGI
- absent hypoglossal nerve / MGI
- abnormal hypoglossal nerve topology / MGI
- absent segment of posterior cerebral artery / MGI
- retropleural edema / MGI
- persistent right 6th pharyngeal arch artery / MGI
- left sided brachiocephalic trunk / MGI
- abnormal vitelline vein topology / MGI
- persistent trigeminal artery / MGI
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