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Index


             alleles, 22–23, 89                Genetic Information
             Aristotle, 19                      Nondiscrimination Act, 91
             autoimmune disorders, 8, 14–17  eugenics, 26–28, 87, 120
               celiac disease, 5             exons, 10, 69, 95
               common variable immune deficiency
                 (CVID), 8–9, 14             fragile X, 65, 71, 124
               Crohn’s disease, 6
               severe combined immunodeficiency   gametes. See sex cells
                 (SCID), 44, 104             gene editing, 6–7, 26, 108, 110, 113,
               type 1 diabetes, 5–6             116–117, 122, 125
                                               CRISPR-Cas9, 110–115
             base pairs, 50–53, 62, 66–67, 69–71, 95  CRISPR-Cas10, 117
                                             genes, 6, 9–10, 18, 22–23, 25, 29–30,
             cancer, 5, 15, 35, 37, 71, 83–84, 95, 101,   50–52, 62–63, 66, 108–109, 123
                 108, 110, 124                 beta-globin gene (HBB), 104, 107
             chromosomes, 10, 13, 20–21, 29–31,   BRCA1, 37
                 52, 58–59, 65–66, 70, 80      BRCA2, 37, 83–84
             codons, 53, 71                    BRCA3, 83–84, 95
             cystic fibrosis (CF), 43, 57–59   BRCA4, 95
                                               CCR5, 114–115
             direct-to-consumer tests, 6, 76, 79,   CFTR, 57–59
                 83–87, 89–91, 95, 98–99, 101  CTLA4, 15–16
               African Ancestry, 85–86         FMR-1, 71
               Ancestry, 85–88, 90, 92, 95     HLA-B51, 17
               Color, 101                      KAT6A, 74–76
               FamilyTreeDNA, 81–82, 91, 93    PAH, 39–40, 47, 53
               Genos, 95–99                    PMM2, 97
               23andMe, 83, 86–88, 90, 92, 94–95,   variants, 9, 13, 22–25, 68–69, 71–74,
                 97–100                         80, 83–86, 89–90, 94–99, 101
             DNA, 13, 26, 50–51, 57–59, 66–68,   gene therapy, 6–7, 103–104, 106–110,
                 71, 79, 89, 103, 107–110, 112–113,   122
                 115–117, 123–124            genetic evidence, 18, 55, 92–93
               mitochondrial, 80–81          genetic sequencing, 6, 40, 51, 57,
               noncoding, 10, 60, 63, 69–70     59–60, 62, 109, 124
               polymerase, 53–54               next-generation sequencing (NGS),
               replication, 53–56               6, 67, 69–72, 74, 77, 101, 109
               structure of, 6, 30–37, 52, 113  Sanger sequencing, 6, 53, 55–56,
               testing, 79, 83–85, 87–88, 90–97,   63, 67
                 95, 99–101. (see also direct-to-  whole exome sequencing, 69–70,
                 consumer tests)                74–76, 95, 101
             dominant, 23–24, 74               whole genome sequencing, 69–70,
                                                72, 76, 95, 101, 103, 114
             epigenetics, 19, 30             genetic testing, 6, 11, 13, 16–17, 21,
             ethics, 6, 76, 84, 86, 114–116, 122  50–51, 61, 65, 67, 75–76, 87, 103,
               ethical, legal, and social issues   118–119, 121–124.
                 (ELSI), 60–61                 See also direct-to-consumer tests)



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