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Symbol
Name
ID
Ctnnb1
catenin beta 1
MGI:88276
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties
Back pain
Lethargy
Autistic behavior
Aggressive behavior
Restlessness
Self-mutilation
Disease(s) Associated with CTNNB1
autosomal dominant intellectual developmental disorder 19
medulloblastoma

Mouse Phenotypes
behavior/neurological phenotype
increased susceptibility to pharmacologically induced seizures
impaired contextual conditioning behavior
abnormal operant conditioning behavior
impaired long-term object recognition memory
enhanced spatial learning
abnormal spatial reference memory
abnormal suckling behavior
increased anxiety-related response
increased thigmotaxis
slow extinction of fear memory
abnormal response to social novelty
increased grooming behavior
impaired coordination
abnormal head movements
stereotypic behavior
abnormal nursing
abnormal nest building behavior
abnormal vocalization
seizures
Availability Mouse Genotype
Ctnnb1Bfc/Ctnnb1+
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Emx1tm1(cre)Yql/Emx1+  (conditional)
Ctnnb1tm2Kem/Ctnnb1tm2Kem
Pvalbtm1(cre)Arbr/Pvalb+  (conditional)
*
Ctnnb1tm1Max/Ctnnb1tm2Kem
Tg(Msx2-cre)5Rem/0  (conditional)

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
05/14/2024
MGI 6.23
The Jackson Laboratory