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Symbol
Name
ID
Ceacam16
CEA cell adhesion molecule 16
MGI:2685615
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Abnormal vestibular function
Sensorineural hearing impairment
Disease(s) Associated with CEACAM16
autosomal dominant nonsyndromic deafness 4B
autosomal recessive nonsyndromic deafness 113

Mouse Phenotypes
absent Hensen stripe
abnormal tectorial membrane striated-sheet matrix morphology
increased or absent threshold for auditory brainstem response
abnormal otoacoustic response
decreased distortion product otoacoustic emission amplitude
decreased distortion product otoacoustic emission threshold
nonsyndromic hearing loss
Availability Mouse Genotype
Ceacam16tm1(KOMP)Wtsi/Ceacam16tm1(KOMP)Wtsi
Ceacam16tm1Wzm/Ceacam16tm1Wzm

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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory