LHFPL5 (gene)

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Lipoma HMGIC fusion partner-like 5 is a protein that in humans is encoded by the LHFPL5 gene. [1]

Function

This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis.

References

  1. "Entrez Gene: Lipoma HMGIC fusion partner-like 5". Retrieved 2016-06-24.

Further reading


This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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