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Antibody detects endogenous levels of total DSS1.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: 26S proteasome complex subunit DSS1; 26S proteasome complex subunit SEM1; Deleted in split hand/split foot protein 1; Deleted in split hand/split foot protein 1 homolog; deleted in split-hand/split-foot 1; split hand/foot deleted gene 1; Split hand/foot deleted protein 1; Split hand/foot deleted protein 1 homolog; Split hand/foot malformation type 1 protein; Split hand/foot malformation type 1 protein homolog
基因别名: C7orf76; DSS1; ECD; SEM1; SHFD1; SHFDG1; Shfg; SHFM1; SHSF1
UniProt ID: (Human) P60896, (Mouse) P60897
Entrez Gene ID: (Human) 7979, (Mouse) 20422, (Rat) 680532