Gene Symbol | SEM1 |
Entrez Gene ID | 7979 |
Full Name | SEM1, 26S proteasome complex subunit |
Synonyms | C7orf76,DSS1,ECD,SHFD1,SHFM1,SHSF1,Shfdg1 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | 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]. |
Disorder MIM: |