ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 24613930	Case ID: 233323T	Disease: Thyroid cancer	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2

	Affected Gene
	PubMed ID: 24613930	Case ID: 233323T	Disease: Thyroid cancer	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description STRN 6801 2 37070783 37193615 striatin, calmodulin binding protein ALK 238 2 29415640 30144432 anaplastic lymphoma receptor tyrosine kinase KLHL29 114818 2 23608088 23931481 kelch-like family member 29 MRPL33 9553 2 27994584 28210954 mitochondrial ribosomal protein L33 BRE 9577 2 28112808 28561768 brain and reproductive organ-expressed (TNFRSF1A modulator) BIRC6 57448 2 32582096 32843966 baculoviral IAP repeat containing 6

Chromothripsis database. 2025 Cai Laboratory