- accession:NM_017929
- 基因别名:PEX26
- 基因描述:Homo sapiens peroxisomal biogenesis factor 26 (PEX26), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:918
- 翻译后氨基酸长度:305
- TranscriptVariant:This variant represents transcript variant 1. Both variants 1 and 2 encode the same isoform (a).
- 基因简介:This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010]
- 载体信息:自有图片地址
- 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