Symbol Name ID |
Lhfpl5
lipoma HMGIC fusion partner-like 5 MGI:1915382 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal vestibular function |
Sensorineural hearing impairment |
Bilateral sensorineural hearing impairment |
Disease(s) Associated with LHFPL5 | |||
autosomal recessive nonsyndromic deafness 67 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal outer hair cell stereociliary bundle morphology |
abnormal cochlear inner hair cell morphology |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
cochlear hair cell degeneration |
organ of Corti degeneration |
increased or absent threshold for auditory brainstem response |
deafness |
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Availability | Mouse Genotype | |||||||||
Lhfpl5hscy-2J/Lhfpl5hscy-2J | ||||||||||
Lhfpl5hscy/Lhfpl5hscy | ||||||||||
Lhfpl5tm1Kjn/Lhfpl5tm1Kjn | ||||||||||
Lhfpl5tm1Kjn/Lhfpl5+ | * |
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 05/14/2024 MGI 6.23 |
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