ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 21215367	Case ID: SNU-C1	Disease: Colorectal cancer	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2 AVEN 15 apoptosis, caspase activation inhibitor PML 15 promyelocytic leukemia RORA 15 RAR-related orphan receptor A USP3 15 ubiquitin specific peptidase 3 RYR3 15 ryanodine receptor 3 PML 15 promyelocytic leukemia RYR3 15 ryanodine receptor 3 TRIM69 15 tripartite motif containing 69 TCF12 15 transcription factor 12 CHD2 15 chromodomain helicase DNA binding protein 2

	Affected Gene
	PubMed ID: 21215367	Case ID: SNU-C1	Disease: Colorectal cancer	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description AVEN 57099 15 34158428 34331377 apoptosis, caspase activation inhibitor CHD2 1106 15 93426526 93571237 chromodomain helicase DNA binding protein 2 IDH2 3418 15 90626277 90645736 isocitrate dehydrogenase 2 (NADP+), mitochondrial PML 5371 15 74287014 74340153 promyelocytic leukemia RORA 6095 15 60780483 61521518 RAR-related orphan receptor A RYR3 6263 15 33603163 34158303 ryanodine receptor 3 SNURF 8926 15 25200133 25223729 SNRPN upstream reading frame TCF12 6938 15 57210821 57591479 transcription factor 12 TRIM69 140691 15 45021186 45060027 tripartite motif containing 69 USP3 9960 15 63796793 63886839 ubiquitin specific peptidase 3

Chromothripsis database. 2025 Cai Laboratory