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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for SHFM1 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID7979
Official gene symbolSHFM1
Full namesplit hand/foot malformation (ectrodactyly) type 1
Aliases,DSS1,ECD,SEM1,SHFD1,SHSF1,Shfdg1,
Gene summaryThe 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]
LocationChromosome: 7   Locus: 7q21.3-q22.1
Gene position96339203 - 96318079  Map Viewer
Gene orientationminus
Gene size21125 bp
Gene sequence
OMIM ID183600