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feingold syndrome
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MIR17HG
Identification and characterization of a novel gene, C13orf25, as a target for 13q31-q32 amplification in malignant lymphoma
MYCN
N-myc amplification in multiple homogeneously staining regions in two human neuroblastomas.
Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage.
Max: a helix-loop-helix zipper protein that forms a sequence-specific DNA-binding complex with Myc
Differential effects of the widely expressed dMax splice variant of Max on E-box vs initiator element-mediated regulation by c-Myc
Cancer Gene Census
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MYCN
Somatic tumors
neuroblastoma, Wilms tumour
Tumor types germline
Cancer Syndrom
Translocation partner
Name
v-myc myelocytomatosis viral related oncogene, neuroblastoma derived (avian)
Chromosome banding
2p24.1
Cancer molecular gen.
Dom
Mutation type
A, Mis
Other syndrome disease
Feingold syndrome 1
Definition
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Pathways
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