Varaico: Literature-Extracted Genetic Variants

Gene:ENAM
Variant:p.I648T
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ENAM

NM_031889.3:p.I648T

Associated Papers

Whole-exome sequencing identifies ECPAS as a novel potentially pathogenic gene in multiple hereditary families with nonsyndromic orofacial cleft.

Zhao H et al.

Protein & Cell, 2024

38695759 (PubMed )
Supplement: pwae021_suppl_supplementary_figures_s1-s10_tables_s1-s2.pdf

Genetic variations in exon 10 of ENAM and their association with early childhood caries.

Sharma A et al.

Journal of Oral Biosciences, 2024

Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.

Bateman NW et al.

Iscience, 2022

35036865 (PubMed )
Supplement: mmc2.xlsx › SupplementalTable1A

Prediction of Early Childhood Caries Based on Single Nucleotide Polymorphisms Using Neural Networks.

Zaorska K et al.

Genes, 2021

ENAM mutations and digenic inheritance.

Zhang H et al.

Molecular Genetics & Genomic Medicine, 2019

Association between ENAM polymorphisms and dental caries in children.

Devang Divakar D et al.

Saudi Journal of Biological Sciences, 2019

Neanderthal and Denisova tooth protein variants in present-day humans.

Zanolli C et al.

Plos One, 2017

Dental caries and enamelin haplotype.

Chaussain C et al.

Journal of Dental Research, 2014

Identification of the enamelin (g.8344delG) mutation in a new kindred and presentation of a standardized ENAM nomenclature.

Hart PS et al.

Archives of Oral Biology, 2003

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."