ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 25161957	Case ID: 25161957_1	Disease: Neuroblastoma	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2

	Affected Gene
	PubMed ID: 25161957	Case ID: 25161957_1	Disease: Neuroblastoma	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description MYCN 4613 2 16080686 16087129 v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog ALK 238 2 29415640 30144432 anaplastic lymphoma receptor tyrosine kinase ATRX 546 X 77504878 77786269 alpha thalassemia/mental retardation syndrome X-linked ARID1A 8289 1 27022524 27108595 AT rich interactive domain 1A (SWI-like) ARID1B 57492 6 157099063 157531913 AT rich interactive domain 1B (SWI1-like)

Chromothripsis database. 2025 Cai Laboratory