Literature DB >> 24634119

A novel rare copy number variant of the ABCF1 gene identified among dengue fever patients from Peninsular Malaysia.

B P Hoh1, S S Sam2, S H Umi3, M Mahiran4, N Y Nik Khairudin5, S Rafidah Hanim6, S Abubakar2.   

Abstract

Copy number variation (CNV) is a form of genetic variation in addition to single nucleotide polymorphisms. The significance of CNV in the manifestation of a number of diseases is only recently receiving considerable attention. We genotyped 163 dengue patients from Peninsular Malaysia for genes possibly linked to dengue infection using quantitative real-time PCR. Here, we report a serendipitous discovery of a novel rare CNV of the ABCF1 gene among the dengue patients. Among these patients, two had a gain of 1 copy (CN = 3) and one had lost 1 copy (CN = 1), indicating that a rare CNV of the ABCF1 gene was detected among dengue patients from Peninsular Malaysia. Although the gene is suspected to regulate inflammatory responses and pathogen-induced cytokine storm, its relevance to dengue requires further investigation.

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Year:  2014        PMID: 24634119     DOI: 10.4238/2014.February.19.9

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  3 in total

1.  Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression.

Authors:  Roman Tremmel; Kathrin Klein; Florian Battke; Sarah Fehr; Stefan Winter; Tim Scheurenbrand; Elke Schaeffeler; Saskia Biskup; Matthias Schwab; Ulrich M Zanger
Journal:  Hum Genet       Date:  2019-11-30       Impact factor: 4.132

2.  Copy number variants of ABCF1, IL17REL, and FCGR3A are associated with the risk of gout.

Authors:  Zheng Dong; Yuan Li; Jingru Zhou; Shuai Jiang; Yi Wang; Yulin Chen; Dongbao Zhao; Chengde Yang; Qiaoxia Qian; Yanyun Ma; Hongjun He; Hengdong Ji; Yajun Yang; Xiaofeng Wang; Xia Xu; Yafei Pang; Hejian Zou; Li Jin; Feng Zhang; Jiucun Wang
Journal:  Protein Cell       Date:  2017-06       Impact factor: 14.870

3.  Targeted exome sequencing of Korean triple-negative breast cancer reveals homozygous deletions associated with poor prognosis of adjuvant chemotherapy-treated patients.

Authors:  Hae Min Jeong; Ryong Nam Kim; Mi Jeong Kwon; Ensel Oh; Jinil Han; Se Kyung Lee; Jong-Sun Choi; Sara Park; Seok Jin Nam; Gyung Yup Gong; Jin Wu Nam; Doo Ho Choi; Hannah Lee; Byung-Ho Nam; Yoon-La Choi; Young Kee Shin
Journal:  Oncotarget       Date:  2017-06-27
  3 in total

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