- accession:NM_001708
- 基因别名:OPN1SW
- 基因描述:Homo sapiens opsin 1 (cone pigments), short-wave-sensitive (OPN1SW), mRNA.
- 载体:现货载体
- CDS区长度:1047
- 翻译后氨基酸长度:348
- 基因简介: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]
- 规格:10ul 质粒
CDS区参考序列: 点击查看序列翻译后氨基酸参数序列: 点击查看序列