NTN1 gene was risk to NSCLO among Han Chinese Population.

ShuYuan Jiang,Jia-Yu Shi,Yan-Song Lin,Shi-Jun Duan, Xieli Chen, Jian-Jun Jiao,Wei Shen, Xiaoju Jin, Miao You, Moyao Wang,Bing Shi,Zhong-Lin Jia

ORAL DISEASES(2019)

引用 11|浏览9
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摘要
Objective Genome-wide association studies (GWAS) found NTN1, NOG and the region between CREBBP and ADCY9 were risks to non-syndromic cleft lip with or without cleft palate (NSCL/P). However, the association of single nucleotide polymorphisms (SNPs) in these genes with NSCL/P in Western China is unknown. Subjects and Methods We selected seven SNPs in NTN1, NOG and between CREBBP and ADCY9, and then performed transmission disequilibrium test (TDT), parent-of-origin effect and sliding window haplotype analysis to test the associations among 302 NSCL/P case-parent trios from Western Han Chinese. Results We found allele G at rs4791774 in NTN1 was significantly overtransmitted among non-syndromic cleft lip only (NSCLO) (p = 0.0067, OR = 1.79, 95% CI: 1.17-2.74); rs4791774 and rs9915089 tightly linked with each other among NSCL/P (D ' = 0.87, r(2) = 0.67) and haplotypes carrying the risk allele G at rs4791774 were always found to be overtransmitted from parents to cases. Motif analysis indicated that allele G at rs4791774 could greatly alter the affinity of Myc_disc7, so allele G at rs4791774 in NTN1 might modulate C-MYC transcription to participate in the aetiology of NSCLO. Conclusions Our study suggested allele G at rs4791774 in NTN1 gene is risk of NSCLO, which could greatly increase the risk to have a baby with cleft.
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关键词
haplotype,non-syndromic cleft lip with or without palate,NTN1,SNPs,transmission disequilibrium test
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