- 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 |
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 |
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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