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LHFPL5

Official Full Name
LHFPL tetraspan subfamily member 5
Organism
Homo sapiens
GeneID
222662
Background
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. [provided by RefSeq, Jul 2008]
Synonyms
TMHS; DFNB67; dJ510O8.8;

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