Sandbox GGC2: Difference between revisions
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== Disease == | == Disease == | ||
There are multiple diseases associated with Human Hexokinase 1. It is possible for illness to arise from a deficiency in the protein. A deficiency is a rare autosomal recessive disease in which the Leucine and Threonine residues in the 529 and the 680 positions are mutated and translated as a Serine. This disease results in nonspherocytic hemolytic anemia<ref>PMID:7655856</ref>. | There are multiple diseases associated with Human Hexokinase 1. It is possible for illness to arise from a deficiency in the protein. A deficiency is a rare autosomal recessive disease in which the <scene name='75/752269/Oliver_leu529/2'>Leucine</scene> and Threonine residues in the 529 and the 680 positions are mutated and translated as a Serine. This disease results in nonspherocytic hemolytic anemia<ref>PMID:7655856</ref>. | ||
== Relevance == | == Relevance == | ||
