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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LHFPL5-20-RE | 20 (40 μL) | 200 μL |  |
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| LHFPL5-20-OR | 20 (40 μL) | 200 μL |  |
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| LHFPL5-20-GO | 20 (40 μL) | 200 μL |  |
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| LHFPL5-20-GR | 20 (40 μL) | 200 μL |  |
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| LHFPL5-20-AQ | 20 (40 μL) | 200 μL |  |
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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 Symbol : LHFPL5
Gene Name : LHFPL tetraspan subfamily member 5
Chromosome : CHR 6: 358,052,93-358,240,74
Locus : 6p21.31
Alt. Genes : FEM1B
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