ChromothripsisDB: a curated database of chromothripsis
 
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  Fusion Gene
  PubMed ID: 25799107 Case ID: Mother2 Disease: Congenital abnormality Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2
 
 
  Affected Gene
  PubMed ID: 25799107 Case ID: Mother2 Disease: Congenital abnormality Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description
AOAH 313 7 36552456 36764154 acyloxyacyl hydrolase (neutrophil)
ANKS1B 56899 12 99120235 100378432 ankyrin repeat and sterile alpha motif domain containing 1B
TRPV4 59341 12 110220890 110271212 transient receptor potential cation channel, subfamily V, member 4
KDM4C 23081 9 6720863 7175648 lysine (K)-specific demethylase 4C
MPDZ 8777 9 13105703 13279589 multiple PDZ domain protein
IFT74 80173 9 26947037 27062928 intraflagellar transport 74
TRDN 10345 6 123537483 123958238 triadin
TLN1 7094 9 35696945 35732392 talin 1
CREB3 10488 9 35732332 35737001 cAMP responsive element binding protein 3
 
Chromothripsis database. 2025 Cai Laboratory