Symbol
Name
ID

Camk2b
calcium/calmodulin-dependent protein kinase II, beta
MGI:88257

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties	Poor appetite	Vocal cord paralysis	Aggressive behavior	Autistic behavior	Bruxism
Disease(s) Associated with CAMK2B
autosomal dominant intellectual developmental disorder 54

Mouse Phenotypes

impaired contextual conditioning behavior

abnormal object recognition memory

decreased anxiety-related response

decreased thigmotaxis

ataxia

impaired balance

impaired coordination

decreased grip strength

abnormal voluntary movement

decreased vertical activity

hyperactivity

abnormal nest building behavior

Availability

Mouse Genotype

Camk2b^tm1.1Ics/Camk2b^tm1.1Ics

Camk2b^tm1Yelg/Camk2b^tm1Yelg

Camk2b^tm1.1Ics/Camk2b⁺

Camk2b^{tm1b(EUCOMM)Hmgu}/Camk2b⁺

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 09/15/2026 MGI 6.29