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LHFPL3 (gene)
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LHFPL3 (gene)
LHFPL tetraspan subfamily member 3 is a protein that in humans is encoded by the LHFPL3 gene.
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 one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. A partial gene fragment named LHFPL4 corresponds to a portion of the first exon of this gene. [provided by RefSeq, Jul 2008].
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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LHFPL3 (gene)
LHFPL tetraspan subfamily member 3 is a protein that in humans is encoded by the LHFPL3 gene.
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 one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. A partial gene fragment named LHFPL4 corresponds to a portion of the first exon of this gene. [provided by RefSeq, Jul 2008].
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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