Symbol Name ID |
Cib2
calcium and integrin binding family member 2 MGI:1929293 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal vestibular function |
Profound sensorineural hearing impairment |
Disease(s) Associated with CIB2 | ||
autosomal recessive nonsyndromic deafness 48 | ||
Usher syndrome type 1J |
Mouse Phenotypes | abnormal inner hair cell kinocilium morphology |
abnormal ear 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 |
abnormal hearing physiology |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
increased or absent distortion product otoacoustic emission threshold |
absent distortion product otoacoustic emissions |
deafness |
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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 04/23/2024 MGI 6.23 |
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