Aliases for SYTL1 Gene
External Ids for SYTL1 Gene
Previous GeneCards Identifiers for SYTL1 Gene
GeneCards Summary for SYTL1 Gene
SYTL1 (Synaptotagmin Like 1) is a Protein Coding gene. Diseases associated with SYTL1 include Deafness, Autosomal Recessive 21 and Autosomal Dominant Nonsyndromic Deafness. Among its related pathways are Vesicle-mediated transport and TBC/RABGAPs. Gene Ontology (GO) annotations related to this gene include calcium ion binding and syntaxin binding. An important paralog of this gene is SYTL2.
UniProtKB/Swiss-Prot for SYTL1 Gene
May play a role in vesicle trafficking (By similarity). Binds phosphatidylinositol 3,4,5-trisphosphate. Acts as a RAB27A effector protein and may play a role in cytotoxic granule exocytosis in lymphocytes (By similarity).