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Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.

作者信息

Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, Pirinen S

机构信息

Institute of Biotechnology, University of Helsinki, Finland.

出版信息

Eur J Hum Genet. 2001 Oct;9(10):743-6. doi: 10.1038/sj.ejhg.5200715.


DOI:10.1038/sj.ejhg.5200715
PMID:11781684
Abstract

Development of dentition is controlled by numerous genes, as has been shown by experimental animal studies and mutations that have been identified by genetic studies in man. Here we report a nonsense mutation in the PAX9 gene that is associated with molar tooth agenesis in a Finnish family. The A340T transversion creates a stop codon at lysine 114, and truncates the coded PAX9 protein at the end of the DNA-binding paired-box. All the affected members of the family were heterozygous for the mutation. The tooth agenesis phenotype involves all permanent second and third molars and most of the first molars and resembles the earlier reported phenotype that was also associated with a PAX9 mutation. The phenotype is presumably a consequence of haploinsufficiency of PAX9. In another Finnish family with molar tooth agenesis, we could not find similar sequence changes in PAX9.

摘要

相似文献

[1]
Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.

Eur J Hum Genet. 2001-10

[2]
A novel mutation in human PAX9 causes molar oligodontia.

J Dent Res. 2002-2

[3]
A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.

Eur J Oral Sci. 2007-8

[4]
Non-syndromic oligodontia with a novel mutation of PAX9.

J Dent Res. 2010-11-22

[5]
Haploinsufficiency of PAX9 is associated with autosomal dominant hypodontia.

Hum Genet. 2002-4

[6]
Novel PAX9 mutations cause non-syndromic tooth agenesis.

J Dent Res. 2014-1-16

[7]
A novel mutation in PAX9 causes familial form of molar oligodontia.

Eur J Hum Genet. 2006-2

[8]
Novel mutation of the initiation codon of PAX9 causes oligodontia.

J Dent Res. 2005-1

[9]
A missense mutation in PAX9 in a family with distinct phenotype of oligodontia.

Eur J Hum Genet. 2003-11

[10]
Mutation of PAX9 is associated with oligodontia.

Nat Genet. 2000-1

引用本文的文献

[1]
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Sci Rep. 2025-8-1

[2]
Association between or gene polymorphism and tooth agenesis risk: A meta-analysis.

Open Life Sci. 2025-4-10

[3]
A novel PAX9 variant in a Chinese family with non-syndromic oligodontia and genotype-phenotype analysis of PAX9variants.

Hua Xi Kou Qiang Yi Xue Za Zhi. 2024-10-1

[4]
Morphometric evaluation of sella turcica and cranial base in patients with congenital absence of teeth.

Hua Xi Kou Qiang Yi Xue Za Zhi. 2022-10-1

[5]
Non-syndromic familial congenital dental deficiency: two cases report.

Hua Xi Kou Qiang Yi Xue Za Zhi. 2022-7-25

[6]
"Examining the link between tooth agenesis and papillary thyroid cancer: is there a risk factor?" Observational study.

Prog Orthod. 2024-3-25

[7]
Genetic Factors of Teeth Impaction: Polymorphic and Haplotype Variants of , , , and Genes.

Int J Mol Sci. 2023-9-9

[8]
Chitosan Hydrogel-Delivered ABE8e Corrects PAX9 Mutant in Dental Pulp Stem Cells.

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[9]
Tooth agenesis patterns and variants in : A systematic review.

Jpn Dent Sci Rev. 2023-12

[10]
Genotype-phenotype pattern analysis of pathogenic variants in Chinese Han families with non-syndromic oligodontia.

Front Genet. 2023-3-28

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