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Phenotypes Associated with This Genotype
Genotype
MGI:2674120
Allelic
Composition
Ctnnb1tm2Kem/Ctnnb1tm2.1Kem
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
involves: 129/Sv * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ctnnb1tm2.1Kem mutation (0 available); any Ctnnb1 mutation (49 available)
Ctnnb1tm2Kem mutation (1 available); any Ctnnb1 mutation (49 available)
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no mutant mice are born

craniofacial
• craniofacial bones derived from neural crest cells are absent
• bones present include optic vesicle, basioccipital, exoccipital

skeleton
• craniofacial bones derived from neural crest cells are absent
• bones present include optic vesicle, basioccipital, exoccipital

nervous system
• shortened neural tube
• brain morphogenesis grossly abnormal between E10.5 and 18.5
• isthmic border between midbrain and rhombencephalon not visible
• choroid plexus absent by E12.5
• by E10.5 parts of the midbrain are missing
• no discernable midbrain by E12.5
• enlarged telencephalon
• walls of cephalic vesicles thinner
• anterior hindbrain is missing by E10.5
• poorly formed connections between cranial ganglia and hindbrain
• cerebellum is missing at E12.5
• anterior hindbrain is missing by E10.5
• combined ganglion with vestibulocochlear nerve abnormal
• roots poorly formed
• hypoglossal nerve missing
• roots poorly formed
• first spinal root ganglion missing
• other spinal root ganglia severely affected as well

embryo
• shortened neural tube


Contributing Projects:
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
04/23/2024
MGI 6.23
The Jackson Laboratory