- abnormal digit morphology / IMPC
- abnormal autopod morphology / IMPC
- abnormal zygomatic bone morphology / IMPC
- abnormal pelvic girdle bone morphology / IMPC
- abnormal brain morphology / IMPC
- abnormal nail morphology / IMPC
- increased lean body mass / IMPC
- abnormal vertebrae morphology / IMPC
- abnormal vertebral arch morphology / IMPC
- increased grip strength / IMPC
- decreased prepulse inhibition / IMPC
- decreased total body fat amount / IMPC
- abnormal cranium morphology / IMPC
C57BL/6N-Twist1tm1.1Arte/Ieg
Status | Available to order |
EMMA ID | EM:05504 |
Citation information | RRID:IMSR_EM:05504 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-Twist1tm1.1Arte/Ieg |
Alternative name | Twist1 KO cond |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Twist1tm1.1 |
Gene/Transgene symbol | Twist1 |
Information from provider
Provider | Helmholtz Zentrum Muenchen |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen German Research Center for Environmental Health (GmbH) |
Genetic information | The complete mouse Twist1 ORF is encoded by exon 1. Exon 1 including 1.5 kb of the promoter region has been flanked by loxP sites, as its genetic ablation should result in loss of function. The conditional targeted mutation has been obtained by in vivo, Flp recombinase-mediated removal of the neomycin selection marker. |
Phenotypic information | TO BE PROVIDED |
Breeding history | Targeting performed in C57BL/6N ES cells and confirmed by Southern blotting. Crossed to C57BL/6N-Tg(CAG-flpe)2Arte mice to obtain mutant founders with excised neo cassette. Maintained on C57BL/6N background. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTac males, wild-type C57BL/6N females |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Saethre-Chotzen syndrome / Orphanet_794
- Isolated scaphocephaly / Orphanet_35093
- Isolated brachycephaly / Orphanet_35099
- Isolated plagiocephaly / Orphanet_35098
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- premature cranial suture closure / MGI
- cleft palate / MGI
- abnormal rib morphology / MGI
- short limbs / MGI
- abnormal forelimb morphology / MGI
- polydactyly / MGI
- abnormal muscle development / MGI
- exencephaly / MGI
- open neural tube / MGI
- decreased body size / MGI
- abnormal gait / MGI
- internal hemorrhage / MGI
- abnormal limb morphology / MGI
- abnormal limb bone morphology / MGI
- premature endochondral bone ossification / MGI
- nervous system phenotype / MGI
- enlarged interparietal bone / MGI
- temporal bone hypoplasia / MGI
- abnormal clavicle morphology / MGI
- craniofacial phenotype / MGI
- skeleton phenotype / MGI
- abnormal bone ossification / MGI
- abnormal osteoblast differentiation / MGI
- short temporal bone squamous part / MGI
- neonatal lethality, complete penetrance / MGI
- embryonic lethality, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- premature coronal suture closure / MGI
- premature lambdoid suture closure / MGI
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