Symbol
Name
ID

Cib2
calcium and integrin binding family member 2
MGI:1929293

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Motor delay
Disease(s) Associated with CIB2	Motor delay
Usher syndrome type 1J

Mouse Phenotypes

abnormal inner hair cell kinocilium morphology

abnormal cochlear hair cell morphology

abnormal inner hair cell stereociliary bundle morphology

abnormal outer hair cell stereociliary bundle morphology

decreased outer hair cell stereocilia number

cochlear hair cell degeneration

abnormal vestibular hair cell stereociliary bundle morphology

decreased vestibular hair cell stereocilia number

abnormal cochlear outer hair cell physiology

absent cochlear microphonics

abnormal hair cell mechanoelectric transduction

decreased prepulse inhibition

Availability

Mouse Genotype

Cib2^em1Xuzg/Cib2^em1Xuzg

Cib2^tm1.1Aela/Cib2^tm1.1Aela

Cib2^{tm1b(EUCOMM)Wtsi}/Cib2^{tm1b(EUCOMM)Wtsi}

Cib2^em1Xuzg/Cib2⁺

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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