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- accession：NM_000276
- 基因别名：OCRL
- 基因描述：Homo sapiens oculocerebrorenal syndrome of Lowe (OCRL), transcript variant a, mRNA.
- 载体：现货载体
- CDS区长度：2706
- 翻译后氨基酸长度：901
- TranscriptVariant：This variant (1) represents the longer transcript and it encodes isoform (a).
- 基因简介：This gene encodes a phosphatase enzyme that is involved in actin polymerization and is found in the trans-Golgi network. Mutations in this gene cause oculocerebrorenal syndrome of Lowe and also Dent disease. [provided by RefSeq, Jul 2008]
- 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
