protein
| binding to PAX7 and FOX01A (concomitant amplification) |
|
modulating MDM2 levels in neuroblastoma cells |
|
interacting with KDM5A, KDM5B and HUWE1 |
|
interaction with HUWE1 (ubiquitin ligase HUWE1 operates upstream of the MYCN-DLL3-NOTCH1 pathway to control neural stem cell activity and promote neurogenesis)  |
|
directly associated with its regulatory motif (E-box) within the putative BIRC7 promoter  |
|
acts directly to repress NTRK1 and NGFR gene transcription  |
|
GSTP1 is a direct transcriptional target of MYCn in neuroblastoma cells  |
|
ALK stimulates initiation of transcription of the MYCN gene  |
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MYCN acts as a direct repressor of the CDKL5 promoter  |
|
SIRT2 enhanced MYCN and MYC protein stability and promoted cancer cell proliferation  |
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cooperation between MYCN and BIRC5 may be important in the genesis of several cancers  |
|
MYCN repressed KDM5B expression by direct binding to the Sp1-binding site-enriched region of the KDM5B gene promoter, and cell proliferation assays showed that transcriptional repression of KDM5B reduced neuroblastoma cell proliferation  |
|
TRIM32 interacted with MYCN at spindle poles during mitosis, facilitating proteasomal degradation of MYCN at spindle poles and inducing Asymmetric cell division (ACD)  |
|
SULF2 is a novel positive regulator of neuroblastoma pathogenicity that contributes to MYCN oncogenicity  |
|
MYCN bound directly to E-boxes within the SKP2 promoter and induced transcriptional activity which was decreased by the removal of MYCN and E-box mutation  |
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MYCN was found to physically interact with and recruit KDM4B  |
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OTX2 is a crucial target of MYCN during inner ear development, and MYCN may directly regulate OTX2  |
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DDX21 induces CEP55 expression, MYCN-amplified neuroblastoma cell proliferation and tumorigenesis  |
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
|  
| amplification
|  
|  
|
in neuroblastoma, amplification is associated with rapid tumor progression and poor prognosis  | tumoral
|  
| amplification
|  
|  
|
in tumors with MYCN amplification and low TPX2 index, a favorable outcome whereas in tumors with normal MYCN copy number and high TPX2 index, the prognosis is extremely poor | tumoral
|  
|  
|  
|  
|
copy number gain is relatively common in Wilms' tumor  | tumoral
|  
| amplification
|  
|  
|
in neuroblastoma  | tumoral
| germinal mutation
|  
|  
| gain of function
|
MYCN gain is a germline aberration, with a significant role for MYCN dysregulation in the molecular biology of Wilms tumour  | tumoral
|  
|  
| --over
|  
|
frequently overexpressed in pediatric T-ALL  | |