半岛bd体育手机客户端 介绍
基因名：
SEM1 半岛bd体育手机客户端 别名： C7orf76； DSS1； ECD； PSMD15； SHFD1； SHFM1； SHSF1； Shfdg1； SEM1； SEM1 26S proteasome subunit； SEM1 26S proteasome subunit； 26S proteasome complex subunit SEM1； 26S proteasome complex subunit DSS1； SEM1 26S proteasome complex subunit； deleted in split hand/split foot protein 1； deleted in split-hand/split-foot 1； split hand/foot deleted protein 1； split hand/foot malformation (ectrodactyly) type 1； split hand/foot malformation type 1 protein； SEM1蛋白亚型2； 先天性裂手/裂足畸形相关蛋白DSS1； 背景信息：
The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]
标签：His-tag |
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