人 LOXHD1 (NM_001145473) cDNA克隆

Accession: NM_001145473
基因名称: LOXHD1
基因别名: LH2D1; DFNB77
基因描述: Homo sapiens lipoxygenase homology domains 1 (LOXHD1), transcript variant 3, mRNA.
种属: Human
CDS区长度: 1539 (查看编码区序列)
翻译后氨基酸长度: 512 (查看氨基酸序列)
Transcript Variant: This variant (3) is missing many exons from the 5' end, and contains an alternate 5' terminal exon compared to variant 1. This results in translation initiation from an in-frame downstream AUG, and a shorter isoform (3) compared to isoform 1.
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G115952 人 LOXHD1 (NM_001145473) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a highly conserved protein consisting entirely of PLAT (polycystin/lipoxygenase/alpha-toxin) domains, thought to be involved in targeting proteins to the plasma membrane. Studies in mice show that this gene is expressed in the mechanosensory hair cells in the inner ear, and mutations in this gene lead to auditory defects, indicating that this gene is essential for normal hair cell function. Screening of human families segregating deafness identified a mutation in this gene which causes DFNB77, a progressive form of autosomal-recessive nonsyndromic hearing loss (ARNSHL). Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Mar 2010]