Symbol Name ID |
Smpx
small muscle protein, X-linked MGI:1913356 |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
High-frequency hearing impairment |
Disease(s) Associated with SMPX | ||
X-linked deafness 4 |
Mouse Phenotypes | abnormal cochlear hair cell stereociliary bundle morphology |
abnormal cochlear outer hair cell morphology |
cochlear outer hair cell degeneration |
increased or absent threshold for auditory brainstem response |
abnormal distortion product otoacoustic emission |
increased susceptibility to noise-induced hearing loss |
nonsyndromic hearing loss |
|
Availability | Mouse Genotype | |||||||
Smpxem1Jgao/Smpxem1Jgao | ||||||||
Smpxem2Jgao/Smpxem2Jgao | ||||||||
Smpxem1Jgao/Smpx+ | ||||||||
Smpxem2Jgao/Smpx+ | ||||||||
Smpxem1Jgao/Y | ||||||||
Smpxem2Jgao/Y |
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 08/02/2024 MGI 6.24 |
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