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| Healthc Inform Res > Volume 28(4); 2022 > Article |
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| Database content | Description | Primary source |
|---|---|---|
| Information about the gene, access to DNA sequence | Users can access the gene name, symbol, gene ID, general description of the gene, and the DNA sequence. | National Library of Medicine [5,21] (https://www.ncbi.nlm.nih.gov/gene) |
| Chromosome location | The location of the gene in the chromosome with its specific cytogenetic position is listed in the database. | OMIM: Online Mendelian Inheritance in Man [20] (https://www.omim.org/) |
| Protein sequence | Users can learn the names of protein(s) encoded by the gene and obtain the entire protein sequence. | National Library of Medicine [21] (https://www.ncbi.nlm.nih.gov/protein/) |
| Three-dimensional protein structure | The dataset provides access to the three-dimensional protein structure and homology models. | AlphaFold Protein Structure Database [16] (https://alphafold.ebi.ac.uk/) |
| Cellular pathways | Users have access to cellular and metabolic pathways where the listed protein is known to play roles. |
Reactome pathway knowledgebase [17] (https://reactome.org/) WikiPathways [18] (https://www.wikipathways.org/) |
| Function of the protein in oral and tooth development | The dental and oral-specific functions of the gene are listed in the database. | PubMed [19] (https://pubmed.ncbi.nlm.nih.gov/) |
| Mutations | Mutations identified in the gene that cause dental and oral diseases are listed in the database. |
OMIM: Online Mendelian Inheritance in Man [20] (https://www.omim.org/) PubMed [19] (https://pubmed.ncbi.nlm.nih.gov/) |
| Dental and oral disease | If a mutation is known to cause an oral or dental disorder, a description of that physiological condition or developmental anomaly is listed in the database. |
OMIM: Online Mendelian Inheritance in Man [20] (https://www.omim.org/) PubMed [19] (https://pubmed.ncbi.nlm.nih.gov/) |
Development of a Standardized Curriculum for Nursing Informatics in Korea2022 October;28(4)

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