Matches in DBpedia 2014 for { <http://dbpedia.org/resource/SHFM1> ?p ?o. }
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- SHFM1 abstract "26S proteasome complex subunit DSS1 is a protein that in humans is encoded by the SHFM1 gene.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.".
- SHFM1 entrezgene "7979".
- SHFM1 wikiPageID "14875820".
- SHFM1 wikiPageRevisionID "593041328".
- SHFM1 hasPhotoCollection SHFM1.
- SHFM1 requireManualInspection "no".
- SHFM1 summaryText "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.".
- SHFM1 updateCitations "yes".
- SHFM1 updatePage "yes".
- SHFM1 updateProteinBox "yes".
- SHFM1 updateSummary "yes".
- SHFM1 type Biomolecule.
- SHFM1 type Protein.
- SHFM1 type BiologicalObject.
- SHFM1 comment "26S proteasome complex subunit DSS1 is a protein that in humans is encoded by the SHFM1 gene.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.".
- SHFM1 label "SHFM1".
- SHFM1 sameAs SHFM1.
- SHFM1 sameAs m.03g_wgn.
- SHFM1 sameAs Q15997144.
- SHFM1 sameAs Q15997144.
- SHFM1 wasDerivedFrom SHFM1?oldid=593041328.
- SHFM1 isPrimaryTopicOf SHFM1.