Gene:
split hand/foot malformation (ectrodactyly) type 1
Gene ID:
202223
Symbol:
SHFM1
Species:
1000
Description:
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.