ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 21215367	Case ID: 8505C	Disease: Thyroid cancer	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2 JAK2 9 Janus kinase 2 TPD52L3 9 tumor protein D52-like 3 MPDZ 9 multiple PDZ domain protein NFIB 9 nuclear factor I/B SMARCA2 9 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 KCNV2 9 potassium channel, voltage gated modifier subfamily V, member 2

	Affected Gene
	PubMed ID: 21215367	Case ID: 8505C	Disease: Thyroid cancer	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description CDKN2A 1029 9 21967751 21995300 cyclin-dependent kinase inhibitor 2A JAK2 3717 9 4985033 5128183 Janus kinase 2 KCNV2 169522 9 2717502 2730037 potassium channel, voltage gated modifier subfamily V, member 2 MLLT3 4300 9 20341663 20622542 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 3 MPDZ 8777 9 13105703 13279589 multiple PDZ domain protein NFIB 4781 9 14081842 14398982 nuclear factor I/B SLC1A1 6505 9 4490444 4587469 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 SMARCA2 6595 9 2015342 2193624 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2 TPD52L3 89882 9 6328349 6331900 tumor protein D52-like 3

Chromothripsis database. 2025 Cai Laboratory