ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 25799107	Case ID: Mother1	Disease: Congenital abnormality	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2

	Affected Gene
	PubMed ID: 25799107	Case ID: Mother1	Disease: Congenital abnormality	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description PTPRD 5789 9 8314246 10612723 protein tyrosine phosphatase, receptor type, D KANK1 23189 9 470291 746105 KN motif and ankyrin repeat domains 1 NRG3 10718 10 83635070 84746935 neuregulin 3

Chromothripsis database. 2025 Cai Laboratory