C57BL/6N-Atm1Brd Cert1tm1a(KOMP)Wtsi/WtsiFlmg
Status | Available to order |
EMMA ID | EM:08488 |
Citation information | RRID:IMSR_EM:08488 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 Cert1tm1a(KOMP)Wtsi/WtsiFlmg |
Alternative name | EPD0855_2_H11 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cert1tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Cert1 |
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 EPD0855_2_H11. 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 | B.S.R.C. Alexander Fleming, Vari, Greece |
Disease and phenotype information
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal heart morphology / MGI
- thin ventricular wall / MGI
- double outlet right ventricle / MGI
- decreased cell proliferation / MGI
- abnormal muscle development / MGI
- abnormal forebrain morphology / MGI
- abnormal cardiovascular system physiology / MGI
- decreased embryo size / MGI
- abnormal lipid homeostasis / MGI
- abnormal nasal cavity morphology / MGI
- abnormal semicircular canal morphology / MGI
- persistent truncus arteriosis / MGI
- absent tibia / MGI
- no phenotypic analysis / MGI
- aphakia / MGI
- fetal growth retardation / MGI
- abnormal optic cup morphology / MGI
- abnormal vertebral arch morphology / MGI
- fusion of vertebral bodies / MGI
- fusion of vertebral arches / MGI
- decreased cervical vertebrae number / MGI
- homeostasis/metabolism phenotype / MGI
- cellular phenotype / MGI
- reproductive system phenotype / MGI
- decreased ventricle muscle contractility / MGI
- abnormal cell physiology / MGI
- abnormal mitochondrion morphology / MGI
- abnormal mitochondrial physiology / MGI
- abnormal cardiac outflow tract development / MGI
- increased heart ventricle size / MGI
- abnormal cervical rib / MGI
- abnormal endoplasmic reticulum morphology / MGI
- abnormal cardiac jelly morphology / MGI
- perimembraneous ventricular septal defect / MGI
- muscular ventricular septal defect / MGI
- abnormal pectinate muscle morphology / MGI
- persistent right dorsal aorta / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal umbilical vein topology / MGI
- abnormal vertebral artery topology / MGI
- heterochrony / MGI
- persistent trigeminal artery / MGI
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