- accession:NM_001108256
- 基因别名:Ocrl
- 基因描述:Rattus norvegicus oculocerebrorenal syndrome of Lowe (Ocrl), mRNA.
- 载体:现货载体
- CDS区长度:2700
- 翻译后氨基酸长度:899
- 基因简介:mutation in human OCRL causes Lowe syndrome, also known as oculocerebrorenal syndrome; mouse homolog RIKEN cDNA 9530014D17 possesses an inositol polyphosphate phosphatase domain [RGD, Feb 2006]
- 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