Results for "Bilateral Foot Drop": 10 genes

Name

BOP Gene

Polymicrogyria, bilateral occipital

SHFLD3 Gene

Split-hand/foot malformation with long bone deficiency 3

SHFLD2 Gene

Split-hand/foot malformation with long deficiency 2

LOC102723422 Gene

foot protein 1 variant 1-like

SHFL1 Gene

Split-hand/foot malformation with long bone deficiency 1

SHFM1P1 Gene

split hand/foot malformation (ectrodactyly) type 1 pseudogene 1

SHFM3 Gene

Split-hand/foot malformation 3

SHFM2 Gene

split hand/foot malformation (ectrodactyly) type 2

SHFM1 Gene

split hand/foot malformation (ectrodactyly) type 1

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]

SHFM5 Gene

split hand/foot malformation (ectrodactyly) type 5