ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 25497101	Case ID: patient 1	Disease: Congenital abnormality	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2 DPYD 1 dihydropyrimidine dehydrogenase ETV1 7 ets variant 1

	Affected Gene
	PubMed ID: 25497101	Case ID: patient 1	Disease: Congenital abnormality	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description DPYD 1806 1 97543299 98386605 dihydropyrimidine dehydrogenase FOXP1 27086 3 71003844 71633140 forkhead box P1 ETV1 2115 7 13930853 14031050 ets variant 1 SNX13 23161 7 17830385 17980124 sorting nexin 13 TMEM106B 54664 7 12250867 12282993 transmembrane protein 106B AHR 196 7 17338246 17385776 aryl hydrocarbon receptor ARL4A 10124 7 12726481 12730559 ADP-ribosylation factor-like 4A

Chromothripsis database. 2025 Cai Laboratory