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Human SHFM1 Knockdown Cell Line-LN428 Glioma

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Cat.No.
CSC-RK0251
Background
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.
Growth Properties
Adherent
Morphology
Epithelial
Host Cell
LN428 glioma
Ship
Dry ice
Gene Information
Official Symbol
SHFM1
Synonyms
SHFM1; split hand/foot malformation (ectrodactyly) type 1; SHFD1; 26S proteasome complex subunit DSS1; deleted in split hand/foot 1; DSS1; ECD; SEM1; Shfdg1; SHSF1; 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;
Gene ID
UniProt ID
P60896
Chromosome Location
7q21.3
Pathway
Homologous recombination, organism-specific biosystem; Homologous recombination, conserved biosystem; Proteasome, organism-specific biosystem; Proteasome, conserved biosystem; Proteasome, 19S regulatory particle (PA700), organism-specific biosystem;
Function
peptidase activity; protein binding;

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