disease:Defects in NBL1 are possibly the cause of the development and/or progression of human neuroblastoma.,function:Possible candidate as a tumor suppressor gene of neuroblastoma. May play an important role in preventing cells from entering the final stage (G1/S) of the transformation process.,similarity:Belongs to the DAN family.,similarity:Contains 1 CTCK (C-terminal cystine knot-like) domain.,tissue specificity:Most abundant in normal lung and meningioma.,
Secreted.
Most abundant in normal lung and meningioma.
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