- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Atm1Brd Prrc2btm1a(EUCOMM)Wtsi/WtsiBiat
Status | Available to order |
EMMA ID | EM:05981 |
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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