- accession:NM_001282677
- 基因别名:PEX1
- 基因描述:Homo sapiens peroxisomal biogenesis factor 1 (PEX1), transcript variant 2, mRNA.
- 载体:现货载体
- CDS区长度:3681
- 翻译后氨基酸长度:1226
- TranscriptVariant:This variant (2) is missing an in-frame coding exon compared to variant 1. The resulting shorter isoform (2) lacks an internal protein segment compared to isoform 1.
- 基因简介:This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013]
- 规格:10ul 质粒
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