TMEM127 : transmembrane protein 127
Description
TMEM127, a gene located on chromosome 17, encodes a transmembrane protein with an unknown function. While its exact role remains elusive, accumulating evidence suggests its involvement in neuronal processes and potential association with neurological disorders. Studies have linked TMEM127 variations to conditions like epilepsy, autism spectrum disorder, and neurodevelopmental delays. Understanding the molecular mechanisms of TMEM127 and its intricate interplay with neuronal pathways could pave the way for novel therapeutic strategies targeting these complex disorders.
Associated Diseases
Did you know?
TMEM127 has been implicated in the regulation of calcium signaling, a critical process for neuronal function.
