ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 22367537	Case ID: N538TL	Disease: Neuroblastoma	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2 BMPR2 2 bone morphogenetic protein receptor, type II (serine/threonine kinase) ERBB4 2 erb-b2 receptor tyrosine kinase 4 EHD3 2 EH-domain containing 3 LTBP1 2 latent transforming growth factor beta binding protein 1 FSHR 2 follicle stimulating hormone receptor WDR75 2 WD repeat domain 75 MSH2 2 mutS homolog 2 SF3B1 2 splicing factor 3b, subunit 1, 155kDa SNTG2 2 syntrophin, gamma 2 GALNT14 2 polypeptide N-acetylgalactosaminyltransferase 14

	Affected Gene
	PubMed ID: 22367537	Case ID: N538TL	Disease: Neuroblastoma	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description CRIM1 51232 2 36583069 36778278 cysteine rich transmembrane BMP regulator 1 (chordin-like) OR4P4 81300 11 55405834 55406772 olfactory receptor, family 4, subfamily P, member 4 POGLUT1 56983 3 119187785 119213555 protein O-glucosyltransferase 1 TMC3 342125 15 81623558 81666554 transmembrane channel-like 3

Chromothripsis database. 2025 Cai Laboratory