ChromothripsisDB: a curated database of chromothripsis
 
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  Fusion Gene
  PubMed ID: 25719666 Case ID: ICGC_0214 Disease: Pancreatic cancer Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2
C2orf88 2 chromosome 2 open reading frame 88 SPAG16 2 sperm associated antigen 16
CCT4 2 chaperonin containing TCP1, subunit 4 (delta) NRXN1 2 neurexin 1
DPY30 2 dpy-30 homolog (C. elegans) GALNT14 2 polypeptide N-acetylgalactosaminyltransferase 14
FAM171B 2 family with sequence similarity 171, member B SPAG16 2 sperm associated antigen 16
GALNT14 2 polypeptide N-acetylgalactosaminyltransferase 14 NRXN1 2 neurexin 1
HPCAL1 2 hippocalcin-like 1 NRXN1 2 neurexin 1
ITGAV 2 integrin, alpha V TM4SF20 2 transmembrane 4 L six family member 20
MREG 2 melanoregulin HIBCH 2 3-hydroxyisobutyryl-CoA hydrolase
MYT1L 2 myelin transcription factor 1-like B3GNT2 2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2
NRXN1 2 neurexin 1 GALNT14 2 polypeptide N-acetylgalactosaminyltransferase 14
SPAG16 2 sperm associated antigen 16 VWC2L 2 von Willebrand factor C domain containing protein 2-like
SPAST 2 spastin NRXN1 2 neurexin 1
TPO 2 thyroid peroxidase DPY30 2 dpy-30 homolog (C. elegans)
 
 
  Affected Gene
  PubMed ID: 25719666 Case ID: ICGC_0214 Disease: Pancreatic cancer Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description
CIR1 9541 2 175212750 175260443 corepressor interacting with RBPJ, 1
HOXD10 3236 2 176973518 176984670 homeobox D10
HOXD11 3237 2 176968944 176974722 homeobox D11
HOXD12 3238 2 176964458 176966408 homeobox D12
HOXD13 3239 2 176957619 176960666 homeobox D13
HOXD9 3235 2 176987088 176989853 homeobox D9
SCRN3 79634 2 175260458 175294303 secernin 3
 
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