人 FAM161A (NM_001201543) cDNA克隆

Accession: NM_001201543
基因名称: FAM161A
基因别名: RP28
基因描述: Homo sapiens family with sequence similarity 161, member A (FAM161A), transcript variant 1, mRNA.
种属: Human
CDS区长度: 2151 (查看编码区序列)
翻译后氨基酸长度: 716 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longer isoform (1).
产品编号 产品名称 载体 规格 价格
G123149 人 FAM161A (NM_001201543) cDNA克隆 pDONR223 2ug质粒 点击询价

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]