Symbol Name ID |
Ceacam16
CEA cell adhesion molecule 16 MGI:2685615 |
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 |
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Availability | Mouse Genotype | |||||||
Ceacam16tm1(KOMP)Wtsi/Ceacam16tm1(KOMP)Wtsi | ||||||||
Ceacam16tm1Wzm/Ceacam16tm1Wzm |
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 04/16/2024 MGI 6.23 |
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