Sandbox Reserved 1737

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Although rare, mutations in the Hexokinase I gene on chromosome 10 can reduce the amount of Hexokinase found in tissues. this reduction has been found to be directly related to early-onset nonspherocytic Hemolytic anemia<ref>McKusick V. HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY. Online Mendelian Inheritance in Man, OMIM®. 1986 Jun.
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Although rare, mutations in the Hexokinase I gene on chromosome 10 can reduce the amount of Hexokinase found in tissues. this reduction has been found to be directly related to early-onset nonspherocytic Hemolytic anemia.<ref>McKusick V. HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY. Online Mendelian Inheritance in Man, OMIM®. 1986 Jun.
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</ref> Other mutations have also been observed causing retinitis pigmentosa, Russe type of hereditary motor and sensory neuropathy, and jaundice. <ref>McKusick V. HEXOKINASE 1; HK1. Online Mendelian Inheritance in Man, OMIM®. 1986 Jun. </ref>
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Other mutations have also been observed causing retinitis pigmentosa, Russe type of hereditary motor and sensory neuropathy, and jaundice. <ref>McKusick V. HEXOKINASE 1; HK1. Online Mendelian Inheritance in Man, OMIM®. 1986 Jun. </ref>
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== References ==
== References ==

Revision as of 04:42, 28 November 2022

This Sandbox is Reserved from August 30, 2022 through May 31, 2023 for use in the course Biochemistry I taught by Kimberly Lane at the Radford University, Radford, VA, USA. This reservation includes Sandbox Reserved 1730 through Sandbox Reserved 1749.
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Hexokinase

Hexokinase Monomer

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