Entrez gene ID | | 7979 |
Official gene symbol | | SHFM1 |
Full name | | split hand/foot malformation (ectrodactyly) type 1 |
Aliases | | ,DSS1,ECD,SEM1,SHFD1,SHSF1,Shfdg1, |
Gene 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] |
Location | | Chromosome: 7 Locus: 7q21.3-q22.1 |
Gene position | | 96339203 - 96318079 Map Viewer |
Gene orientation | | minus |
Gene size | | 21125 bp |
Gene sequence |
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OMIM ID | | 183600 |