an individual who has the genotype hbshba has the phenotype of:,

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The genotype hbshba is a rare genetic mutation that has the phenotype of:, but only about 1 in 10,00 people have it. The HBSHBA gene codes for an enzyme called beta-glucosidase which processes certain sugars and carbohydrates. If you have this gene you may be more at risk for developing type 2 diabetes or celiac disease, though it is not always possible to know if someone will develop these conditions without further testing. Keywords: phenotypes, genotypes, hbshba Body: The genotype HBSHBA is a rare genetic mutation that has the phenotype of, but only about one in ten thousand people have it. The HBSHBA gene codes for an enzyme called beta-glucosidase which processes certain sugars and carbohydrates. If you have this gene you may be more at risk for developing type two diabetes or celiac disease, though it is not always possible to know if someone will develop these conditions without further testing. As with any other trait, however, there’s no way of knowing who will possess the gene until they are tested – many individuals could carry its DNA sequence yet never show symptoms because their bodies lack some necessary enzyme to

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