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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
C2cd3tm1c(EUCOMM)Wtsi
targeted mutation 1c, Wellcome Trust Sanger Institute
MGI:6887626
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
C2cd3tm1c(EUCOMM)Wtsi/C2cd3tm1c(EUCOMM)Wtsi
E2f1Tg(Wnt1-cre)2Sor/E2f1+
involves: C3H * C57BL/6 MGI:6887948


Genotype
MGI:6887948
cn1
Allelic
Composition
C2cd3tm1c(EUCOMM)Wtsi/C2cd3tm1c(EUCOMM)Wtsi
E2f1Tg(Wnt1-cre)2Sor/E2f1+
Genetic
Background
involves: C3H * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
C2cd3tm1c(EUCOMM)Wtsi mutation (0 available); any C2cd3 mutation (101 available)
E2f1Tg(Wnt1-cre)2Sor mutation (2 available); any E2f1 mutation (28 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• midline widening detected at e11.5 which is exacerbated at E15.5

cellular
• increased Gli3FL/Gli3R ratio indicating the cilia are functionally impaired

skeleton
• delayed ossification of the palatine and sphenoid bones at E17.5

digestive/alimentary system

growth/size/body
• midline widening detected at e11.5 which is exacerbated at E15.5





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory