- failure of vascular branching / MGI
- distended pericardium / MGI
- abnormal pontine flexure morphology / MGI
- abnormal somite development / MGI
- decreased embryo size / MGI
- abnormal visceral yolk sac morphology / MGI
- abnormal umbilical cord morphology / MGI
- abnormal neural tube morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal vitelline vasculature morphology / MGI
- abnormal forebrain development / MGI
- small first pharyngeal arch / MGI
- abnormal paraxial mesoderm morphology / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- delayed heart development / MGI
- absent intersomitic vessels / MGI
B6;129P2-Adam10tm2Psa/Ph
| Status | Available to order |
| EMMA ID | EM:07449 |
| Citation information | RRID:IMSR_EM:07449 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;129P2-Adam10tm2Psa/Ph |
| Alternative name | Adam10flox |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Adam10tm2Psa |
| Gene/Transgene symbol | Adam10 |
Information from provider
| Provider | Paul Saftig |
| Provider affiliation | Institute of Biochemistry, Christian-Albrechts-University Kiel |
| Genetic information | A mouse cosmid clone containing the 5' region of the Adam10 gene with exon 2 was isolated from a 129/Ola cosmid library. For construction of the targeting vector, an 8.2 kb KpnI-PstI DNA restriction fragment of Adam10 covering exon 2 was subcloned into the plasmid vector pUC-18. The hygromycin B resistance gene, driven by PGK promoter flanked with two flippase recognition target sequences, one loxP sequence downstream of the hygromycin B resistance gene, was inserted into NotI-ApaI site 5' upstream of exon2 into intron1. A second loxP sequence was inserted into the SphI-SpeI site in intron 2. The targeting vector was linearized and introduced into ES cell line E14 129P2/OlaHsd. Mutated ES cell lines were microinjected into blastocysts of C57BL/6J mice. |
| Phenotypic information | Adam10floxed mice do not show specific phenotype, they have normal habitus and appearance. |
| Breeding history | After ES cell injection into 129/SvEv Adam10 flox mice were backcrossed 3 times onto C57BL/6N background. Colony is now maintained on C57BL/6NCrl background. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Reticulate acropigmentation of Kitamura / Orphanet_178307
MGI phenotypes (gene matching)
Literature references
- The disintegrin/metalloproteinase ADAM10 is essential for the establishment of the brain cortex.;Jorissen Ellen, Prox Johannes, Bernreuther Christian, Weber Silvio, Schwanbeck Ralf, Serneels Lutgarde, Snellinx An, Craessaerts Katleen, Thathiah Amantha, Tesseur Ina, Bartsch Udo, Weskamp Gisela, Blobel Carl P, Glatzel Markus, De Strooper Bart, Saftig Paul, ;2010;The Journal of neuroscience : the official journal of the Society for Neuroscience;30;4833-44; 20371803
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