ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 25043231	Case ID: DGAP259	Disease: Congenital abnormality	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2

	Affected Gene
	PubMed ID: 25043231	Case ID: DGAP259	Disease: Congenital abnormality	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description CNTN6 27255 3 1134260 1445901 contactin 6 TBC1D5 9779 3 17198654 18486309 TBC1 domain family, member 5 CNTNAP2 26047 7 145813453 148118090 contactin associated protein-like 2 PTPRD 5789 9 8314246 10612723 protein tyrosine phosphatase, receptor type, D L3MBTL4 91133 18 5954705 6415236 l(3)mbt-like 4 (Drosophila) WDR7 23335 18 54318574 54698828 WD repeat domain 7

Chromothripsis database. 2025 Cai Laboratory