ChromothripsisDB: a curated database of chromothripsis
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	Fusion Gene
	PubMed ID: 28260531	Case ID: UTR22	Disease: Autism spectrum disorder	Genome Assembly: GRCh37/hg19
Gene Symbol 1 Chromosome1 Description 1 Gene Symbol 2 Chromosome2 Description 2

	Affected Gene
	PubMed ID: 28260531	Case ID: UTR22	Disease: Autism spectrum disorder	Genome Assembly: GRCh37/hg19
Gene Symbol Entrez Gene Chromosome Start End Description WIPF1 7456 2 175424300 175547644 WAS/WASL interacting protein family, member 1 XIRP2 129446 2 167744997 168116263 xin actin-binding repeat containing 2 ZNF385B 151126 2 180306709 180726232 zinc finger protein 385B ACO1 48 9 32384618 32454767 aconitase 1, soluble NSMAF 8439 8 59496063 59572403 neutral sphingomyelinase (N-SMase) activation associated factor FRMPD1 22844 9 37650997 37746901 FERM and PDZ domain containing 1 KIAA1715 80856 2 176788620 176867567 KIAA1715 TOX 9760 8 59717977 60031767 thymocyte selection-associated high mobility group box UBAP2 55833 9 33921691 34048947 ubiquitin associated protein 2 SCN9A 6335 2 167051695 167232503 sodium channel, voltage gated, type IX alpha subunit SCN7A 6332 2 167260083 167350757 sodium channel, voltage gated, type VII alpha subunit

Chromothripsis database. 2025 Cai Laboratory