Predicted to be located in cytoplasmic vesicle; membrane; and synapse. Expressed in head and intestine. Human ortholog(s) of this gene implicated in DOORS syndrome; epilepsy (multiple); and nonsyndromic deafness (multiple). Is an ortholog of human TBC1D24 (TBC1 domain family member 24).
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.