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- accession：NM_001587
- 基因别名：OCRL
- 基因描述：Homo sapiens oculocerebrorenal syndrome of Lowe (OCRL), transcript variant b, mRNA.
- 载体：现货载体
- CDS区长度：2682
- 翻译后氨基酸长度：893
- TranscriptVariant：This variant (2) lacks an alternate in-frame exon, compared to variant 1, resulting in a shorter protein (isoform 2) that has a shorter C-terminus, compared to isoform 1.
- 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
