Automated description from the Alliance of Genome Resources (Release 7.5.0)
Predicted to enable microtubule binding activity and olfactory receptor binding activity. Involved in regulation of intracellular transport. Located in endoplasmic reticulum membrane and endoplasmic reticulum tubular network. Is expressed in diaphragm; nervous system; neural retina; and skeletal musculature. Used to study hereditary spastic paraplegia 31. Human ortholog(s) of this gene implicated in autosomal dominant distal hereditary motor neuronopathy 12; autosomal recessive distal hereditary motor neuronopathy 6; and hereditary spastic paraplegia 31. Orthologous to human REEP1 (receptor accessory protein 1).
This site uses cookies.
Some cookies are essential for site operations and others help us analyze use and utility of our web site.
Please refer to our
privacy policy
for more information.