Homework Clinic
Science Clinic => Biology => Topic started by: burchfield96 on Jan 12, 2022
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Two databases, OMIM and Mitomap, are especially useful in exploring human mitochondrial mutations. If you are interested in learning whether aminoglycoside-induced deafness is inherited maternally, and what gene(s) is/are involved, which of the following would give you the most information?
◦ the Mitomap position map with gene names
◦ the sequence with specifically altered amino acid coding
◦ the OMIM description of symptoms and diagnosis
◦ the OMIM description of the TRMU gene at 22q13
◦ the Mitomap loci of genes associated with deafness
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the Mitomap loci of genes associated with deafness