×
![]()
- accession：NM_032180
- 基因别名：FAM161A
- 基因描述：Homo sapiens family with sequence similarity 161, member A (FAM161A), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：1983
- 翻译后氨基酸长度：660
- TranscriptVariant：This variant (2) lacks an in-frame coding exon and encodes a shorter isoform (2), as compared to isoform 1.
- 基因简介：This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011]
- 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
