- short tail / MGI
- decreased vertebrae number / MGI
- truncated notochord / MGI
- postnatal lethality / MGI
- abnormal primitive node morphology / MGI
- abnormal motile primary cilium morphology / MGI
- decreased embryonic cilium length / MGI
- abnormal embryonic cilium location or orientation / MGI
- absent nodal flow / MGI
STOCK Nototm1Gos/Kctt
| Status | Available to order |
| EMMA ID | EM:10371 |
| Citation information | RRID:IMSR_EM:10371 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 | STOCK Nototm1Gos/Kctt |
| Alternative name | Nototm1Gos |
| Strain type | Targeted Mutant Strains : Knock-in |
| Allele/Transgene symbol | Nototm1Gos |
| Gene/Transgene symbol | Noto |
Information from provider
| Provider | Achim Gossler |
| Provider affiliation | Medizinische Hochschule Hannover |
| Genetic information | Knock-in of GFP into the Noto locus. |
| Phenotypic information | Homozygous:Disruption of l- r- asymmetry of visceral organs.Heterozygous:none |
| References |
|
| Homozygous fertile | no |
| Homozygous viable | no |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Karolinska Institutet, Stockholm, Sweden |
| Animals used for archiving | heterozygous mixed males |
Disease and phenotype information
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal vertebrae morphology / MGI
- kinked tail / MGI
- short tail / MGI
- hindlimb paralysis / MGI
- abnormal floor plate morphology / MGI
- abnormal dorsal root ganglion morphology / MGI
- decreased caudal vertebrae number / MGI
- abnormal blood vessel morphology / MGI
- abnormal somite development / MGI
- abnormal left-right axis patterning / MGI
- postnatal lethality / MGI
- premature death / MGI
- abnormal tail morphology / MGI
- curly tail / MGI
- absent tail / MGI
- abnormal primitive node morphology / MGI
- abnormal motile primary cilium morphology / MGI
- fusion of vertebral bodies / MGI
- decreased vertebrae number / MGI
- decreased lumbar vertebrae number / MGI
- truncated notochord / MGI
- embryo phenotype / MGI
- skeleton phenotype / MGI
- abnormal sclerotome morphology / MGI
- abnormal motile primary cilium physiology / MGI
- decreased embryonic cilium length / MGI
- abnormal embryonic cilium location or orientation / MGI
- absent nodal flow / MGI
Literature references
- The mouse homeobox gene Not is required for caudal notochord development and affected by the truncate mutation.;Abdelkhalek Hanaa Ben, Beckers Anja, Schuster-Gossler Karin, Pavlova Maria N, Burkhardt Hannelore, Lickert Heiko, Rossant Janet, Reinhardt Richard, Schalkwyk Leonard C, Müller Ines, Herrmann Bernhard G, Ceolin Marcelo, Rivera-Pomar Rolando, Gossler Achim, ;2004;Genes & development;18;1725-36; 15231714
- The mouse homeobox gene Noto regulates node morphogenesis, notochordal ciliogenesis, and left right patterning.;Beckers Anja, Alten Leonie, Viebahn Christoph, Andre Philipp, Gossler Achim, ;2007;Proceedings of the National Academy of Sciences of the United States of America;104;15765-70; 17884984
- Differential regulation of node formation, nodal ciliogenesis and cilia positioning by Noto and Foxj1.;Alten Leonie, Schuster-Gossler Karin, Beckers Anja, Groos Stephanie, Ulmer Bärbel, Hegermann Jan, Ochs Matthias, Gossler Achim, ;2012;Development (Cambridge, England);139;1276-84; 22357932
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