BTNL2 Gene and prostate cancer susceptibility
Edited by:Mohammad Hezarkhani MD,Urologist
Board-Certified of Urology,Tehran University ,The Member of Iranian Urological Association
Madaen Hospital Tehran Iran
Mohammad.hezarkhani@yahoo.com
www.Hezarkhani.blogfa.com hosted in Washington DC, United States
september,6 , 2013
Background: Location : 6p21.3
Sequence : Chromosome: 6; NC_000006.11 (32362513..32374900, complement)
GeneRIFs: Gene References Into Functions
5.The BTNL2 A allele variant occurs with a high frequency in Danish patients with sarcoidosis
10.Single-nucleotide polymorphism in the BTNL2 gene is associated with ulcerative colitis.
Rare, inherited mutations account for 5% to 10% of all prostate cancer cases. However, to date, few causative mutations have been identified.Results indicate that rare BTNL2 variants play a role in susceptibility to both familial and sporadic prostate cancer.
References:
1- Germline Missense Variants/ BTNL2 Gene/Associated with Prostate Cancer Susceptibility
Liesel M. FitzGerald1, Akash Kumar2, Evan A. Boyle2, Yuzheng Zhang1,1, Suzanne Kolb1,
Marni Stott-Miller1, Tiffany Smith4, Danielle M. Karyadi4, Elaine A. Ostrander4Li Hsu1,
Jay Shendure2, and Janet L. Stanford1,3/Authors' Affiliations: 1Division of Public Health Sciences, Fred Hutchinson Cancer Research Center; 2Department of Genome Sciences, School of Medicine, 3Department of Epidemiology, School of Public Health, University of Washington, Seattle, Washington; and 4Cancer Genetics Branch, National Human Genome Research Institute, NIH, Bethesda, Maryland June 23, 2013. ©2013 American Association for Cancer Research.
2- National Center for Biotechnology Information, U.S. National Library of Medicine 8600 Rockville Pike, Bethesda MD, 20894 USA/August.21.2013
بنام خداوند طراح معماها