Detection and analysis of common pathogenic germline mutations in Peutz-Jeghers syndrome

doi:10.3748/wjg.v27.i39.6631

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Oct 21, 2021 (publication date) through Jun 8, 2024

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Basic Study

World J Gastroenterol. Oct 21, 2021; 27(39): 6631-6646
Published online Oct 21, 2021. doi: 10.3748/wjg.v27.i39.6631

Table 2 Cancer genetic susceptibility 139 gene panel coverage

AIP	CYLD	FANCL	MLH3	PRSS1	SMARCA4
ALK	DDB2	FANCM	MRE11A	PTCH1	SMARCB1
APC	DICER1	FAS	MSH2	PTCH2	SMARCE1
ATM	DIS3L2	FH	MSH6	PTEN	SOS1
ATR	EGFR	FLCN	MTAP	PTPN11	STAT3
AXIN2	ELANE	GALNT12	MTUS1	RAD50	STK11
BAP1	EPCAM	GATA2	MUTYH	RAD51B	SUFU
BARD1	ERCC1	GEN1	NBN	RAD51C	TERT
BLM	ERCC2	GJB2	NF1	RAD51D	TGFBR1
BMPR1A	ERCC3	GPC3	NF2	RB1	TMEM127
BRCA1	ERCC4	GREM1	NSD1	RECQL	TP53
BRCA2	ERCC5	HMBS	NTRK1	RECQL4	TSC1
BRIP1	EXT1	HNF1A	PALB2	RET	TSC2
BUB1B	EXT2	HOXB13	PALLD	RHBDF2	UROD
CBL	EZH2	HRAS	PDGFRA	RUNX1	USHBP1
CDC73	FANCA	KIT	PHOX2B	SBDS	VEGFA
CDH1	FANCB	LASP1	PMS1	SDHA	VHL
CDK4	FANCC	MAX	PMS2	SDHAF2	WRN
CDKN1B	FANCD2	MC1R	POLD1	SDHB	WT1
CDKN1C	FANCE	MEN1	POLE	SDHC	XPA
CDKN2A	FANCF	MET	POLH	SDHD	XPC
CEBPA	FANCG	MTTF	PPM1D	SLX4	XRCC2
CHEK1	FANCI	MLH1	PRKAR1A	SMAD4	ZMAT3
CHEK2

Citation: Gu GL, Zhang Z, Zhang YH, Yu PF, Dong ZW, Yang HR, Yuan Y. Detection and analysis of common pathogenic germline mutations in Peutz-Jeghers syndrome. World J Gastroenterol 2021; 27(39): 6631-6646
URL: https://www.wjgnet.com/1007-9327/full/v27/i39/6631.htm
DOI: https://dx.doi.org/10.3748/wjg.v27.i39.6631