ChromothripsisDB: a curated database of chromothripsis
 
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  Fusion Gene
  PubMed ID: 23583981 Case ID: SJLGG039 Disease: Glioma Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2
FYCO1 3 FYVE and coiled-coil domain containing 1 RAF1 3 Raf-1 proto-oncogene, serine/threonine kinase
ST6GAL1 3 ST6 beta-galactosamide alpha-2,6-sialyltranferase 1 WHSC1 4 Wolf-Hirschhorn syndrome candidate 1
UBE2J2 1 ubiquitin-conjugating enzyme E2, J2 PKD1 16 polycystic kidney disease 1 (autosomal dominant)
 
 
  Affected Gene
  PubMed ID: 23583981 Case ID: SJLGG039 Disease: Glioma Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description
ABCC5 10057 3 183637722 183735803 ATP-binding cassette, sub-family C (CFTR/MRP), member 5
CYTH3 9265 7 6201407 6312275 cytohesin 3
FYCO1 79443 3 45959396 46037316 FYVE and coiled-coil domain containing 1
KDM2A 22992 11 66886740 67025558 lysine (K)-specific demethylase 2A
PHLDB1 23187 11 118477155 118528741 pleckstrin homology-like domain, family B, member 1
PKD1 5310 16 2138711 2185899 polycystic kidney disease 1 (autosomal dominant)
RAF1 5894 3 12625100 12705725 Raf-1 proto-oncogene, serine/threonine kinase
SLIT1 6585 10 98757795 98945677 slit homolog 1 (Drosophila)
ST6GAL1 6480 3 186648274 186796341 ST6 beta-galactosamide alpha-2,6-sialyltranferase 1
TP73 7161 1 3569084 3652765 tumor protein p73
UBE2J2 118424 1 1189289 1209265 ubiquitin-conjugating enzyme E2, J2
WHSC1 7468 4 1873151 1983934 Wolf-Hirschhorn syndrome candidate 1
 
Chromothripsis database. 2025 Cai Laboratory