Symbol Name ID |
Ctnnb1
catenin beta 1 MGI:88276 |
* | 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 |
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Availability | Mouse Genotype | ||||||||||||||||||||
Ctnnb1Bfc/Ctnnb1+ | |||||||||||||||||||||
Ctnnb1tm2Kem/Ctnnb1tm2Kem Emx1tm1(cre)Yql/Emx1+ (conditional) |
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Ctnnb1tm2Kem/Ctnnb1tm2Kem Pvalbtm1(cre)Arbr/Pvalb+ (conditional) |
* | ||||||||||||||||||||
Ctnnb1tm1Max/Ctnnb1tm2Kem Tg(Msx2-cre)5Rem/0 (conditional) |
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 |
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