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Symbol Name ID |
Ctnnb1
catenin beta 1 MGI:88276 |
| Darker colors indicate more annotations |
| Human Phenotypes | Spasticity |
Spastic diplegia |
Progressive spasticity |
Hypotonia |
| Disease(s) Associated with CTNNB1 | ||||
| autosomal dominant intellectual developmental disorder 19 |
| Mouse Phenotypes | abnormal muscle development |
abnormal tendon morphology |
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| Availability | Mouse Genotype | ||
| Ctnnb1tm1Mmt/Ctnnb1tm1Mmt H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Ctnnb1tm1Yy/Ctnnb1tm1Yy Tg(Prrx1-cre)1Cjt/0 (conditional) |
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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 04/16/2024 MGI 6.23 |
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