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]
Accession: | NM_001108256 |
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基因名称: | Ocrl |
基因描述: | Rattus norvegicus oculocerebrorenal syndrome of Lowe (Ocrl), mRNA. |
种属: | Rat |
CDS区长度: | 2700 (查看编码区序列) |
翻译后氨基酸长度: | 899 (查看氨基酸序列) |
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]