Symbol Name ID |
Cabp2
calcium binding protein 2 MGI:1352749 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hearing impairment |
Disease(s) Associated with CABP2 | |
autosomal recessive nonsyndromic deafness 93 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal cochlear inner hair cell physiology |
abnormal hearing electrophysiology |
abnormal auditory brainstem response |
abnormal auditory brainstem response waveform shape |
increased or absent threshold for auditory brainstem response |
|
Availability | Mouse Genotype | ||||||
Cabp2em1(IMPC)J/Cabp2em1(IMPC)J | |||||||
Cabp2tm1b(KOMP)Mbp/Cabp2tm1b(KOMP)Mbp | * |
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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