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Symbol
Name
ID

Cabp2
calcium binding protein 2
MGI:1352749

Phenotype annotations related to hearing/vestibular/ear

*	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	Hearing impairment
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	hearing/vestibular/ear phenotype	abnormal cochlear inner hair cell physiology	abnormal hearing electrophysiology	abnormal auditory brainstem response	abnormal auditory brainstem response waveform shape
	Cabp2^em1(IMPC)J/Cabp2^em1(IMPC)J
	Cabp2^{tm1b(KOMP)Mbp}/Cabp2^{tm1b(KOMP)Mbp}	*

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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