SHFM1

• Official Symbol: SEM1
• Official Name: SEM1 26S proteasome complex subunit
• Aliases and Previous Symbols: N/A
• Entrez ID: 7979
• UniProt: Q6ZVN7"|"P60896|Q6ZVN7"
• Interactions: BioGRID
• PubMed articles: Open PubMed
• OMIM: Open OMIM

• Entrez 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].
• UniProt Summary: N/A

Pfam Domains GO Terms

Compound Hit Most Correlated Genes in Chemogenomics Tissues where Essential in the Avana Dataset (DepMap 20Q1)

• Essentiality Rank: 2380
• Expression level (log2 read counts): 6.02

Expression Distribution

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SHFM1 Expression in NALM6 Cells: 6.02