Symbol Name ID |
Crbn
cereblon MGI:1913277 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Attention deficit hyperactivity disorder |
Self-injurious behavior |
Disease(s) Associated with CRBN | ||
autosomal recessive intellectual developmental disorder 2 |
Mouse Phenotypes | behavior/neurological phenotype |
impaired contextual conditioning behavior |
impaired spatial learning |
abnormal long-term spatial reference memory |
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Availability | Mouse Genotype | ||||
Crbntm1.2Jjh/Crbntm1.2Jjh | * | ||||
Crbntm1Csp/Crbntm1Csp | * | ||||
Crbntm1.1Jjh/Crbntm1.1Jjh Tg(Camk2a-cre)T29-1Stl/0 (conditional) |
* | ||||
Crbntm1.1Jjh/Crbntm1.1Jjh (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 05/21/2024 MGI 6.23 |
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