×
![]()
- accession：NM_001164716
- 基因别名：PYGM
- 基因描述：Homo sapiens phosphorylase, glycogen, muscle (PYGM), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：2265
- 翻译后氨基酸长度：754
- TranscriptVariant：This variant (2) lacks two exons uses an alternate in-frame splice site in the 5' coding region compared to variant 1. The resulting protein (isoform 2) is shorter compared to isoform 1.
- 基因简介：This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]
- 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
