Automated description from the Alliance of Genome Resources (Release 3.1.1)
Predicted to contribute to nucleosome binding activity. Involved in dendritic cell dendrite assembly; dendritic spine development; and neuron-neuron synaptic transmission. Localizes to nBAF complex. Is expressed in several structures, including alimentary system; brain; genitourinary system; respiratory system; and sensory organ. Used to study Coffin-Siris syndrome 1 and autism spectrum disorder. Human ortholog(s) of this gene implicated in Coffin-Siris syndrome; Coffin-Siris syndrome 1; intellectual disability; and neuroblastoma. Orthologous to human ARID1B (AT-rich interaction domain 1B).