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Mutations Vocabulary 1. mutation—a change in the DNA code 2. gene mutation—affects the smallest amount of DNA 3. point mutation (or substitution)—gene mutation in which a change in a single base; affects only one codon 4. frameshift insertion—gene mutation in which one or more bases are added 5. frameshift deletion— gene mutation in which one or more bases are deleted 6. chromosomal mutation—piece of a chromosome breaks off and can reattach 7. chromosomal insertion/duplication—chromosomal mutation in which part of a chromatid is attached to its sister chromatid causing a duplication of genes 8. chromosomal deletion—chromosomal mutation in which part of a chromosome is lost 9. chromosomal inversion—chromosomal mutation in which part is inverted (or backwards); may affect only a short sequence of code 10. chromosomal translocation—chromosomal mutation in which part is translocated (moved) to a different chromosome 11. nondisjunction—failure of homologous chromosomes to separate properly during cell division 12. karyotype—a chart of chromosome pairs used to diagnose certain genetic disorders 13. monosomy—nondisjunction in which only ONE chromosome of a pair is inherited 14. trisomy—nondisjunction in which THREE chromosomes are inherited instead of two 15. triploidy—nondisjunction in which an EXTRA SET of chromosomes is inherited 16. pedigree—chart used to analyze the inheritance of a certain trait in a family 17. autosomal—a trait that is NOT sex-linked 18. autosomes—body chromosomes