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LHFPL5, LHFPL tetraspan subfamily member 5

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LHFPL5, LHFPL tetraspan subfamily member 5

  • 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]

  • Gene Synonyms (LHFPL tetraspan subfamily member 5 protein, LHFP-like protein 5, lipoma HMGIC fusion partner-like 5 protein, tetraspan membrane protein of hair cell stereocilia, DFNB67, TMHS, dJ510O8.8,)
  • NCBI Gene ID: 222662
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q8TAF8
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

LHFPL tetraspan subfamily member 5 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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