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 DomainsGO Terms
Pfam Domains
No Pfam Domain information is available for this gene.
GO Terms
proteasome regulatory particle, lid subcomplex
proteasome assembly
double-strand break repair via homologous recombination
recombinational repair
mRNA-containing ribonucleoprotein complex export from nucleus
mRNA export from nucleus
ribonucleoprotein complex export from nucleus
ribonucleoprotein complex localization
RNA export from nucleus
protein export from nucleus
mRNA transport
nuclear export
double-strand break repair
RNA transport
nucleic acid transport
establishment of RNA localization
RNA localization
DNA recombination
nucleobase-containing compound transport
protein-containing complex localization
nucleocytoplasmic transport
nuclear transport
DNA repair
DNA metabolic process
cellular response to DNA damage stimulus
cellular protein-containing complex assembly
intracellular protein transport
protein transport
intracellular transport
peptide transport
protein-containing complex assembly
amide transport
cellular protein localization
cellular macromolecule localization
establishment of protein localization
cellular response to stress
establishment of localization in cell
nitrogen compound transport
protein-containing complex subunit organization
gene expression
CRISPR Data
Compound HitMost Correlated Genes in ChemogenomicsTissues where Essential in the Avana Dataset (DepMap 20Q1)