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Symbol
Name
ID
Smpx
small muscle protein, X-linked
MGI:1913356
Phenotype annotations related to hearing/vestibular/ear
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

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
04/23/2024
MGI 6.23
The Jackson Laboratory