- 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
STOCK Loxl3tm1a(EUCOMM)Wtsi/Cnbc
Status | Available to order |
EMMA ID | EM:13124 |
Citation information | RRID:IMSR_EM:13124 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 Loxl3tm1a(EUCOMM)Wtsi/Cnbc |
Alternative name | APC |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Loxl3tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Loxl3 |
Information from provider
Provider | Francisco Portillo |
Provider affiliation | Biochemistry, Universidad Autonoma de Madrid |
Additional owner | Amparo Cano and Patricia G Santamaria, Universidad Autónoma de Madrid, Madrid, Spain |
Genetic information | Targeted mutation in the Loxl3 gene. ES cell clones containing a targeted mutation of Loxl3 (Loxl3tm1a(EUCOMM)Wtsi, conditional ready, null/knockout, reporter - cre recombinase/loxP system) were obtained from the EUCOMM repository. |
Phenotypic information | Homozygous:Partial perinatal lethality due to osteo-articular defects.Heterozygous:None |
Breeding history | ES clones cells containing a targeted mutation of Loxl3 (Loxl3tm1a(EUCOMM)Wtsi, conditional ready, null/knockout, reporter - cre recombinase/loxP system) were obtained from the EUCOMM repository. Heterozygous animals were intercrossed to obtain homozygous animals. |
References |
|
Homozygous fertile | no |
Homozygous viable | no |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous mixed males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive Stickler syndrome / Orphanet_250984
MGI phenotypes (gene matching)
Literature references
- Loxl2 and Loxl3 Paralogues Play Redundant Roles during Mouse Development.;Santamaría Patricia G, Dubus Pierre, Bustos-Tauler José, Floristán Alfredo, Vázquez-Naharro Alberto, Morales Saleta, Cano Amparo, Portillo Francisco, ;2022;International journal of molecular sciences;23;; 35628534
Information on how we integrate external resources can be found here
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