NP_006295.1
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NCBI GenBank Nucleotide #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
8,278 Da
NCBI Official Full Name
26S proteasome complex subunit DSS1
NCBI Official Synonym Full Names
split hand/foot malformation (ectrodactyly) type 1
NCBI Official Synonym Symbols
ECD; DSS1; SEM1; SHFD1; SHSF1; Shfdg1 [Similar Products]
NCBI Protein Information
26S proteasome complex subunit DSS1; split hand/foot deleted protein 1; deleted in split-hand/split-foot 1; deleted in split hand/split foot protein 1; split hand/foot malformation type 1 protein
UniProt Protein Name
26S proteasome complex subunit DSS1
UniProt Synonym Protein Names
Deleted in split hand/split foot protein 1; Split hand/foot deleted protein 1; Split hand/foot malformation type 1 protein
UniProt Synonym Gene Names
UniProt Entry Name
DSS1_HUMAN
NCBI Summary for SHFM1
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]
UniProt Comments for SHFM1
SHFM1: Subunit of the 26S proteasome which plays a role in ubiquitin-dependent proteolysis. Belongs to the DSS1/SEM1 family.
Protein type: Proteasome complex; DNA repair, damage; Protease
Chromosomal Location of Human Ortholog: 7q21.3
Cellular Component: proteasome complex; integrator complex
Molecular Function: protein binding
Biological Process: double-strand break repair via homologous recombination
Disease: Split-hand/foot Malformation 1
Research Articles on SHFM1
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Products associated with SHFM1 elisa kit
Pathways associated with SHFM1 elisa kit
Diseases associated with SHFM1 elisa kit
Organs/Tissues associated with SHFM1 elisa kit
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