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Pathways
Genes search result for Homo sapiens
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3 records found for search term Shfm1
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
733723DLX5distal-less homeobox 5This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the fami79702039697024831Human262old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1349756SEM1SEM1 26S proteasome subunitThe 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 f79648162696709846Human112description , old_gene_symbolgene, protein-coding, REVIEWED [RefSeq]
1626597SEM1P1SEM1 pseudogene 158189243881892891Humanold_gene_symbolgene, pseudo, INFERRED [RefSeq]