B6;129S-Cert1tm1Jsau/Cnbc
| Status | Available to order |
| EMMA ID | EM:08304 |
| Citation information | RRID:IMSR_EM:08304 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 | B6;129S-Cert1tm1Jsau/Cnbc |
| Alternative name | Kin-LoxPe11-GPBP-1 |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Cert1tm1Jsau |
| Gene/Transgene symbol | Cert1 |
Information from provider
| Provider | Juan Bautista Saus Mas |
| Provider affiliation | Bioquímica y Biología Molecular., Universidad de Valencia. Facultad de Medicina. |
| Genetic information | Targeted insertion of a loxP site between exons 10 and 11 as well as a floxed neomycin resistance cassette between exons 11 and 12. The loxP site between exons 10 and 11 was inserted using a PCR strategy. |
| Phenotypic information | Homozygous:There is no evident phenotype in this strain.Heterozygous:There is no evident phenotype in this strain. |
| Breeding history | To generate floxed Cert1 (GPBP-1) mice, previously obtained (neo+/loxP+) 129/SvEv ES cells transfected with a suitable replacement vector, were injected into C57BL/6 blastocysts. The resulting chimeric mice were further crossed to obtain homozygous (neo+/loxP+) mice. Later they were backcrossed to C57BL/6 and maintained during several years. There is no specific information about the number of generations backcrossed and sib-mated. |
| References |
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| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | yes |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
| Animals used for archiving | homozygous unknown males, homozygous unknown females |
| Stage of embryos | 2-cell |
Disease and phenotype information
IMPC phenotypes (gene 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
Literature references
- Goodpasture antigen-binding protein (GPBP) directs myofibril formation: identification of intracellular downstream effector 130-kDa GPBP-interacting protein (GIP130).;Revert-Ros Francisco, López-Pascual Ernesto, Granero-Moltó Froilán, Macías Jesús, Breyer Richard, Zent Roy, Hudson Billy G, Saadeddin Anas, Revert Fernando, Blasco Raül, Navarro Carmen, Burks Deborah, Saus Juan, ;2011;The Journal of biological chemistry;286;35030-43; 21832087
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