| Background: |
disease:Defects in CAMTA1 are detected in patients with oligodendroglioma and astrocytoma.,function:Transcriptional activator. May act as a tumor suppressor.,induction:Detected at low levels at interphase and in resting cells. Up-regulated during S-phase and mitosis. Levels decrease at the end of mitosis.,similarity:Belongs to the CAMTA family.,similarity:Contains 1 CG-1 DNA-binding domain.,similarity:Contains 1 IPT/TIG domain.,similarity:Contains 3 ANK repeats.,similarity:Contains 3 IQ domains.,subunit:May interact with calmodulin .,tissue specificity:Detected in whole brain, cerebellum, brain cortex, occipital lobe, frontal lobe, temporal lobe, putamen, heart and kidney. Detected in neuroblastic-type cultured neuroblastoma cells., |
