- persistence of hyaloid vascular system / IMPC
- irregularly shaped pupil / IMPC
- decreased circulating phosphate level / IMPC
- impaired pupillary reflex / IMPC
- abnormal placement of pupils / IMPC
- abnormal retina blood vessel morphology / IMPC
- abnormal retina morphology / IMPC
- abnormal locomotor behavior / IMPC
B6.129P2-Sema3etm1Ddg/Orl
| Status | Available to order |
| EMMA ID | EM:01373 |
| Citation information | RRID:IMSR_EM:01373 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-Sema3etm1Ddg/Orl |
| Alternative name | Sema3E |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Sema3etm1Ddg |
| Gene/Transgene symbol | Sema3e |
Information from provider
| Provider | Christopher Henderson |
| Provider affiliation | INSERM UMR 623 - IBDM |
| Genetic information | The first coding exon of mouse Sema3e encodes the signal peptide. In the targeting vector, a DNA fragment encoding the green fluorescent protein EGFP is inserted exactly at the start codon of the Sema3e gene. The vector also contains a neo cassette flanked by loxP sites for ES cell selection. This vector was used to target the Sema3e locus by homologous recombination in ES cells and generate the mutant locus. Recombinant ES cells were injected into C57BL/6 blastocysts. Chimeric founders were bred to C57BL/6 mice, and heterozygous mice were crossed with cre recombinase-expressing mice in order to delete the neo-cassette. Finally heterozygous mice were used to establish lines that were backcrossed to either a C57BL/6 or a CD1 genetic background. |
| Phenotypic information | nothing |
| Breeding history | Five backcrosses to C57BL/6. |
| References |
|
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
| Animals used for archiving | heterozygous C57BL/6J males, wild-type C57BL/6J females |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal motor neuron morphology / MGI
- abnormal motor neuron innervation pattern / MGI
- abnormal retina morphology / MGI
- abnormal somite development / MGI
- abnormal retinal vasculature morphology / MGI
- nervous system phenotype / MGI
- behavior/neurological phenotype / MGI
- abnormal intersomitic vessel morphology / MGI
- Bergmeister's papilla / MGI
Literature references
- Semaphorin 3E and plexin-D1 control vascular pattern independently of neuropilins.;Gu Chenghua, Yoshida Yutaka, Livet Jean, Reimert Dorothy V, Mann Fanny, Merte Janna, Henderson Christopher E, Jessell Thomas M, Kolodkin Alex L, Ginty David D, ;2005;Science (New York, N.Y.);307;265-8; 15550623
- Sema3E-PlexinD1 signaling selectively suppresses disoriented angiogenesis in ischemic retinopathy in mice.;Fukushima Yoko, Okada Mitsuhiro, Kataoka Hiroshi, Hirashima Masanori, Yoshida Yutaka, Mann Fanny, Gomi Fumi, Nishida Kohji, Nishikawa Shin-Ichi, Uemura Akiyoshi, ;2011;The Journal of clinical investigation;121;1974-85; 21505259
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