How do we know that mutations occur randomly?
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
17. Mutation, Repair, and Recombination
Types of Mutations
Problem A.2a
Textbook Question
Go online to the Online Mendelian Inheritance of Man (OMIM) website. Look up the following genetic conditions and answer the questions posed about them.
Look up Tay–Sachs disease (TSD), OMIM number 272800, and give the name and abbreviation of the affected gene and the chromosome location of the gene.

1
Go to the Online Mendelian Inheritance in Man (OMIM) website at https://omim.org/.
Use the search bar on the OMIM homepage to enter the OMIM number '272800' or the disease name 'Tay–Sachs disease'.
Navigate to the Tay–Sachs disease entry page that appears in the search results.
On the Tay–Sachs disease page, locate the section that lists the gene(s) associated with the condition. Identify the gene name and its standard abbreviation.
Find the chromosome location information for the gene, which is usually provided as a cytogenetic band (e.g., 15q23) or a specific chromosome number and region.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Online Mendelian Inheritance in Man (OMIM) Database
OMIM is a comprehensive, authoritative online database cataloging human genes and genetic disorders. It provides detailed information about gene functions, mutations, and associated phenotypes, making it an essential tool for genetic research and clinical diagnosis.
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Gene Nomenclature and Abbreviations
Genes are identified by standardized names and abbreviations that reflect their function or discovery history. Understanding gene symbols helps in accurately locating and referencing specific genes, such as HEXA for Tay–Sachs disease, facilitating clear communication in genetics.
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Chromosomal Location of Genes
Each gene resides at a specific position on a chromosome, described by chromosome number and locus. Knowing the chromosomal location, like HEXA on chromosome 15 for Tay–Sachs, is crucial for genetic mapping, diagnosis, and understanding inheritance patterns.
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