Tbc1d24 - TBC1 domain family, member 24

Involved in positive regulation of dendrite morphogenesis; positive regulation of excitatory postsynaptic potential; and positive regulation of neuron migration. Predicted to be located in several cellular components, including neuromuscular junction; plasma membrane; and terminal bouton. Human ortholog(s) of this gene implicated in DOORS syndrome; epilepsy (multiple); and nonsyndromic deafness (multiple). Orthologous to human TBC1D24 (TBC1 domain family member 24). [provided by Alliance of Genome Resources, Apr 2022]