Symbol Name ID |
Cib2
calcium and integrin binding family member 2 MGI:1929293 |
Darker colors indicate more annotations |
Human Phenotypes | Motor delay |
Disease(s) Associated with CIB2 | |
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 |
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Availability | Mouse Genotype | ||||||||||||
Cib2em1Xuzg/Cib2em1Xuzg | |||||||||||||
Cib2tm1.1Aela/Cib2tm1.1Aela | |||||||||||||
Cib2tm1b(EUCOMM)Wtsi/Cib2tm1b(EUCOMM)Wtsi | |||||||||||||
Cib2em1Xuzg/Cib2+ |
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 09/03/2024 MGI 6.24 |
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