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Distribution of the CCR5 Gene 32-basepair Deletion in 11 Chinese Populations

Bibliographic Data

ID3778617
AuthorsChunyu Zhang (0000-0002-3590-9164, Harbin Medical University), Songbin Fu (0000-0003-0382-9888), Yali Xue (0000-0002-4501-6909), Qi Wang (0000-0003-0464-2118), Xiaoyi Huang (0009-0002-1636-0214), Baiqiu Wang (0000-0001-7356-6767), An Liu (0000-0001-9453-0894), Linlin Ma (0000-0002-1281-4728), Yang Yu (0000-0001-5353-6165), Rongqiuan Shi, Fuqu Fv, Zongcheng Shi, Yu Zhang (0000-0002-0059-270X), Wenhong Cheng (0000-0003-4469-9442), Qionghua Ai (0000-0001-5947-0160), Fang Xu (0000-0001-8201-1595), Chengbin Huang (0009-0000-8890-2727), Baibin Chen, Xianghua Kang, Yanyang Sun, Guiyin Zhang (0000-0003-3851-1263), Pu Li (0000-0001-7771-5598)
Year2002
Volume60
Issue3
Pages267-271
Publication date2002-09-13
Peer ReviewedYes
Open AccessNo
TypeARTICLE
VenueAnthropologischer Anzeiger (JOURNAL)
Journal identifiersISSN: 0003-5548 • E-ISSN: 2363-7099
PublisherS ch we iz er ba rt (PUBLISHER)
DOI10.1127/anthranz/60/2002/267
PMID12378793
OpenAlexW143554126
LanguageEN

A mutant allele of the chemokine receptor gene CCR5 bearing a 32-basepair deletion (delta 32CCR5) could increase the resistance to HIV-1 infection or delayed progression to AIDS. The frequency of this mutation is higher in Europeans than in Asians. To investigate the distribution of this polymorphism in China, 715 individuals from 11 Chinese populations were screened by PCR, including the Han and 10 other ethnic groups. The delta 32CCR5 gene was found in 16 individuals from 5 ethnic groups. All of them were heterozygous. The frequency of the mutant alleles of delta 32CCR5 is low in China and reflects (or might reflect) ancestral gene flow from Europe to Chinese ethnic groups and recent intermarriage within the ethnic groups.

Allele · Allele frequency · Biology · China · Ethnic group · Gene · Gene flow · Genetic variation · Geography · Mutant · Polymorphism (computer science) · Sociology · Genetics · HIV Research and Treatment · Immune Cell Function and Interaction · Immunodeficiency and Autoimmune Disorders

Citation velocityhistorical
Highly citedNo
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