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Article

Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men.

Human molecular genetics - 1 Jun 2012

Lin Xiaoling, Lu Daru, Gao Yong, Tao Sha, Yang Xiaobo, Feng Junjie, Tan Aihua, Zhang Haiying, Hu Yanling, Qin Xue, Kim Seong-Tae, Peng Tao, Li Li, Mo Linjian, Zhang Shijun, Trent Jeffrey M, Mo Zengnan, Zheng S Lilly, Xu Jianfeng, Sun Jielin

Abstract excerpt

Vitamin B12 (VitB12 or cobalamin) is an essential cofactor in several metabolic pathways. Clinically, VitB12 deficiency is associated with pernicious anemia, neurodegenerative disorder, cardiovascular disease and gastrointestinal disease. Although previous genome-wide association studies (GWAS) identified several genes, including FUT2, CUBN, TCN1 and MUT, that may influence VitB12 levels in European populations,...

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Source

Identifiers

PMID: 22367966
DOI: 10.1093/hmg/dds062

Genes

FUT2
CLYBL
CUBN
FUT6
TCN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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