Automated description from the Alliance of Genome Resources (Release 7.4.0)
Predicted to enable damaged DNA binding activity. Predicted to be involved in double-strand break repair via homologous recombination; negative regulation of double-strand break repair via nonhomologous end joining; and spindle organization. Predicted to be located in site of DNA damage. Predicted to be active in centrosome and spindle pole. Is expressed in liver lobe; midbrain ventricular layer; olfactory cortex ventricular layer; and telencephalon ventricular layer. Orthologous to human AUNIP (aurora kinase A and ninein interacting protein).
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