KEGG   ORTHOLOGY: K09109Help
Entry
K09109                      KO                                     

Name
NMYC, MYCN
Definition
N-myc proto-oncogene protein
Pathway
Transcriptional misregulation in cancer
Disease
H00043  
Neuroblastoma
H00510  
Feingold syndrome
Brite
KEGG Orthology (KO) [BR:ko00001]
 Human Diseases
  Cancers
   05202 Transcriptional misregulation in cancers
    K09109  NMYC, MYCN; N-myc proto-oncogene protein
Transcription factors [BR:ko03000]
 Eukaryotic Type
  Basic helix-loop-helix/leucine zipper (bHLH-ZIP)
   Cell cycle controlling factors, Myc
    K09109  NMYC, MYCN; N-myc proto-oncogene protein
BRITE hierarchy
Genes
HSA: 
4613(MYCN)
PTR: 
459043(MYCN)
PPS: 
100975833(MYCN)
GGO: 
101144030(MYCN)
PON: 
100454633(MYCN)
MCC: 
698699(MYCN)
MCF: 
102117042(MYCN)
MMU: 
18109(Mycn)
RNO: 
298894(Mycn)
CGE: 
HGL: 
TUP: 
102471178(MYCN)
CFA: 
482978(MYCN)
AML: 
FCA: 
101093013(MYCN)
PTG: 
BTA: 
616888(MYCN)
BOM: 
102287886(MYCN)
PHD: 
102322264(MYCN)
CHX: 
102186408(MYCN)
OAS: 
101105814(MYCN)
SSC: 
100518190(MYCN)
CFR: 
102506595(MYCN)
BACU: 
103006984(MYCN)
LVE: 
103072014(MYCN)
ECB: 
100146296(MYCN)
MYB: 
102252877(MYCN)
MYD: 
102762085(MYCN)
PALE: 
102878063(MYCN)
OAA: 
100086701(MYCN)
GGA: 
421948(MYCN)
MGP: 
APLA: 
101802792(MYCN)
TGU: 
100226985(MYCN)
FAB: 
101806106(MYCN)
PHI: 
102102251(MYCN)
FPG: 
101910369(MYCN)
FCH: 
102047324(MYCN)
CLV: 
102098538(MYCN)
ASN: 
102382862(MYCN)
AMJ: 
PSS: 
102443952(MYCN)
CMY: 
102947344(MYCN)
ACS: 
100566282(mycn)
PBI: 
103066988(MYCN)
XLA: 
100337516(mycn-b) 380041(mycn-a)
XTR: 
448649(mycn)
DRE: 
252851(mycn)
TRU: 
MZE: 
OLA: 
XMA: 
LCM: 
CMK: 
103180961(mycn)
TCA: 
 » show all
TaxonomyKoalaUniProt
Reference
  Authors
Hurlin PJ
  Title
N-Myc functions in transcription and development.
  Journal
Birth Defects Res C Embryo Today 75:340-52 (2005)

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