Symbol
Name
ID

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

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

Mouse Phenotypes

behavior/neurological phenotype

abnormal behavior

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^tm2.1Yelg/Camk2b^tm2.1Yelg

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)
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