ChromothripsisDB: a curated database of chromothripsis
 
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  Fusion Gene
  PubMed ID: 22367537 Case ID: N752TL Disease: Neuroblastoma Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2
 
 
  Affected Gene
  PubMed ID: 22367537 Case ID: N752TL Disease: Neuroblastoma Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description
BRD7 29117 16 50347398 50402845 bromodomain containing 7
CCDC108 255101 2 219867568 219906249 coiled-coil domain containing 108
CGNL1 84952 15 57668165 57842925 cingulin-like 1
DICER1 23405 14 95552565 95624347 dicer 1, ribonuclease type III
DOPEY2 9980 21 37529080 37666572 dopey family member 2
MS4A4A 51338 11 60048014 60076445 membrane-spanning 4-domains, subfamily A, member 4A
ORAI2 80228 7 102073553 102097268 ORAI calcium release-activated calcium modulator 2
RGS5 8490 1 163080911 163291577 regulator of G-protein signaling 5
SORCS3 22986 10 106400859 107024993 sortilin-related VPS10 domain containing receptor 3
TRAPPC6A 79090 19 45666186 45681495 trafficking protein particle complex 6A
UBE4A 9354 11 118230300 118269926 ubiquitination factor E4A
ZNF133 7692 20 18269121 18297640 zinc finger protein 133
 
Chromothripsis database. 2025 Cai Laboratory