Nexmif - neurite extension and migration factor Gene

Also known as Xpn; KIDLIA; A230051P11

About Nexmif

Summary

Predicted to be involved in negative regulation of cell adhesion and negative regulation of neuron migration. Predicted to act upstream of or within nervous system development. Predicted to be located in several cellular components, including midbody; mitotic spindle; and nucleoplasm. Predicted to be active in nucleus. Is expressed in several structures, including brain; neural tube mantle layer; sensory organ; skeleton; and tarsus. Used to study autism spectrum disorder and non-syndromic X-linked intellectual disability 98. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability 98. Orthologous to human NEXMIF (neurite extension and migration factor). [provided by Alliance of Genome Resources, Apr 2022]