- short mandible / MGI
- abnormal vomer bone morphology / MGI
- cleft palate / MGI
- abnormal vertebral body morphology / MGI
- abnormal craniofacial morphology / MGI
- abnormal pulmonary alveolus morphology / MGI
- no phenotypic analysis / MGI
- abnormal chest morphology / MGI
- abnormal spine curvature / MGI
- abnormal vertebral column morphology / MGI
- abnormal vertebral body development / MGI
- cardiovascular system phenotype / MGI
- respiratory system phenotype / MGI
- vision/eye phenotype / MGI
- abnormal palate development / MGI
- failure of palatal shelf elevation / MGI
- palatal shelves fail to meet at midline / MGI
- integument phenotype / MGI
- postnatal lethality, complete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
C57BL/6N-Loxl3tm1a(EUCOMM)Wtsi/H
| Status | Available to order |
| EMMA ID | EM:09699 |
| Citation information | RRID:IMSR_EM:09699 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-Loxl3tm1a(EUCOMM)Wtsi/H |
| Alternative name | EPD0336_7_H09 |
| Strain type | Targeted Mutant Strains |
| Allele/Transgene symbol | Loxl3tm1a(EUCOMM)Wtsi |
| Gene/Transgene symbol | Loxl3 |
| 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 | MRC, Medical Research Council |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | This mouse line originates from EUCOMM ES clone EPD0336_7_H09. For further details on the construction of this clone see the page at the IKMC portal. |
| Phenotypic information | Potential phenotyping data in the IMPC portal |
| References | None available |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive Stickler syndrome / Orphanet_250984
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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