ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 23915422	Case ID: 23915422_1	Disease: Congenital heart defects	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2

	Affected Gene
	PubMed ID: 23915422	Case ID: 23915422_1	Disease: Congenital heart defects	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description HSD11B2 3291 16 67464555 67471456 hydroxysteroid (11-beta) dehydrogenase 2

© 2015 Cai Laboratory.  Last updated on 13 Mar 2018