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- accession：NM_032753
- 基因别名：QRX; ARMD6; RAXL1; CORD11
- 基因描述：Homo sapiens retina and anterior neural fold homeobox 2 (RAX2), mRNA.
- 载体：现货载体
- CDS区长度：555
- 翻译后氨基酸长度：184
- 基因简介：This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. [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
