Neurensin-1 (NRSN1)

Neurensin-1 (NRSN1) is a small, membrane-associated protein encoded by the NRSN1 gene on human chromosome 6[1][3][6]. It is predominantly expressed in neural tissues, where it localizes to transport vesicles, growth cones, neuron projections, and neuronal cell bodies[2][3][6]. Neurensin-1 is predicted to play a key role in nervous system development, neural organelle transport, nerve signal transduction, neurite extension, and memory consolidation[1][6]. Mutations or dysregulation of NRSN1 are associated with several neurodevelopmental disorders, including dyslexia and conditions marked by eye movement abnormalities and ataxia[1]. Currently, there are no known drugs that directly target Neurensin-1, and it is not classified as a conventional therapeutic target such as a receptor or enzyme[1][6].

Other names

Vesicular membrane protein p24VMPNeuro-p24Vesicular membrane protein of 24 kDaneurensin-1neuro-p24vesicular membrane protein p24vesicular membrain protein p24NRSN1