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Explain Sickle Cell Amenia
Mutation in humans, are sometimes found in the gene, which creates haemoglobin for red blood cells. This gives the different shape to the haemoglobin molecule. In this disease, during translation on chromosome 11 one base is substituted for another so that the codon GAG in the normal sense strand gives glu.ac (glutamic acid) and is substituted in the mutated sense strand becoming GTG giving val (valine.).

*Symptoms = weakness, fatigue, and shortness of breath. Because oxygen cannot be carried as efficiently by the irregular blood cells, the haemoglobin tends to crystallize within the red blood cells, causing them to be flexible. The affected red blood cells can get stuck in the capillaries so blood flow can be slowed or blocked.

Mostly found in populations originating from West Africa or from the Mediterranean. People affected by sickle cell have a risk of passing the mutated gene to their offspring.