人 OPN1SW (NM_001708) cDNA克隆

Accession: NM_001708
基因名称: OPN1SW
基因别名: BCP; BOP; CBT
基因描述: Homo sapiens opsin 1 (cone pigments), short-wave-sensitive (OPN1SW), mRNA.
种属: Human
CDS区长度: 1047 (查看编码区序列)
翻译后氨基酸长度: 348 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G157242 人 OPN1SW (NM_001708) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008]