External Ids for SNX7 Gene
Previous GeneCards Identifiers for SNX7 Gene
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region like some family members, and its exact function is unknown. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 11. [provided by RefSeq, Jun 2010]
GeneCards Summary for SNX7 Gene
SNX7 (Sorting Nexin 7) is a Protein Coding gene. Diseases associated with SNX7 include Spastic Paraplegia 29, Autosomal Dominant and Charcot-Marie-Tooth Disease, Type 4B3. Gene Ontology (GO) annotations related to this gene include phosphatidylinositol binding. An important paralog of this gene is SNX30.
UniProtKB/Swiss-Prot Summary for SNX7 Gene
May be involved in several stages of intracellular trafficking.