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Symbol
Name
ID

Lhfpl5
lipoma HMGIC fusion partner-like 5
MGI:1915382

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	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
Availability	Mouse Genotype	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		deafness
	Lhfpl5^hscy-2J/Lhfpl5^hscy-2J
	Lhfpl5^hscy/Lhfpl5^hscy
	Lhfpl5^tm1Kjn/Lhfpl5^tm1Kjn
	Lhfpl5^tm1Kjn/Lhfpl5⁺	*

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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