ChromothripsisDB: a curated database of chromothripsis
 
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  Fusion Gene
  PubMed ID: 26031834 Case ID: Pa102C Disease: Pancreatic cancer Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2
 
 
  Affected Gene
  PubMed ID: 26031834 Case ID: Pa102C Disease: Pancreatic cancer Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description
C18orf54 162681 18 51884287 51911588 chromosome 18 open reading frame 54
CCDC68 80323 18 52568740 52626739 coiled-coil domain containing 68
DCC 1630 18 49866542 51057784 DCC netrin 1 receptor
DYNAP 284254 18 52254988 52266724 dynactin associated protein
ELAC1 55520 18 48494361 48514491 elaC ribonuclease Z 1
MAPK4 5596 18 48086448 48258194 mitogen-activated protein kinase 4
MBD2 8932 18 51679079 51751158 methyl-CpG binding domain protein 2
ME2 4200 18 48405419 48474691 malic enzyme 2, NAD(+)-dependent, mitochondrial
MEX3C 51320 18 48700920 48744674 mex-3 RNA binding family member C
MRO 83876 18 48324574 48351772 maestro
POLI 11201 18 51795774 51847636 polymerase (DNA directed) iota
RAB27B 5874 18 52385091 52562747 RAB27B, member RAS oncogene family
SMAD4 4089 18 48494410 48611415 SMAD family member 4
STARD6 147323 18 51850728 51884334 StAR-related lipid transfer (START) domain containing 6
TCF4 6925 18 52889562 53332018 transcription factor 4
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