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ENO3

  • ENO3

    • Protein-coding gene in the species Homo sapiens

    Enolase 3 (ENO3), more commonly known as beta-enolase (ENO-β), is an enzyme that in humans is encoded by the ENO3 gene. This gene encodes one of the three

    ENO3

    ENO3

    ENO3

  • Enolase

    • Enzyme involved in glycolysis

    humans, deficiency of ENO1 is linked to hereditary haemolytic anemia, while ENO3 deficiency is linked to glycogen storage disease type XIII. Enolase is a

    Enolase

    Enolase

    Enolase

  • Oncogenomics

    • Sub-field of genomics

    approach to GBM inhibition. ENO1 is one of three homologous genes (ENO2, ENO3) that encodes the mammalian alpha-enolase enzyme. ENO2, which encodes enolase

    Oncogenomics

    Oncogenomics

    Oncogenomics

  • Alpha-enolase

    • Protein found in humans

    ENO1 is one of three enolase isoforms, the other two being ENO2 (ENO-γ) and ENO3 (ENO-β). Each isoform is a protein subunit that can hetero- or homodimerize

    Alpha-enolase

    Alpha-enolase

    Alpha-enolase

  • Glycogen storage disease

    • Medical condition

    Rhabdomyolysis. Hemolytic anemia and other symptoms GSD XIII / GSD 13 β-enolase (ENO3) ? No ? No Exercise intolerance, cramps Increasing intensity of myalgias

    Glycogen storage disease

    Glycogen storage disease

    Glycogen_storage_disease

  • Enolase deficiency

    • Medical condition

    total enolase activity in muscle.[citation needed] Two mutations in the ENO3 gene, the gene encoding β-enolase, is responsible for the deficiency, both

    Enolase deficiency

    Enolase_deficiency

  • List of human protein-coding genes 3

    • HGNC:28388; Q8TC29 4954 ENO1 HGNC:3350; P06733 4955 ENO2 HGNC:3353; P09104 4956 ENO3 HGNC:3354; P13929 4957 ENO4 HGNC:31670; A6NNW6 4958 ENOPH1 HGNC:24599; Q9UHY7

    List of human protein-coding genes 3

    List_of_human_protein-coding_genes_3

  • Inborn errors of carbohydrate metabolism

    • Medical condition

    unclear role. See respective conditions. See respective conditions Enolase 3 ENO3 131370 Muscle GSD type XIII (GSD 13, β-enolase deficiency, beta-enolase deficiency

    Inborn errors of carbohydrate metabolism

    Inborn errors of carbohydrate metabolism

    Inborn_errors_of_carbohydrate_metabolism

  • List of OMIM disorder codes

    • storage disease XII; 611881; ALDOA Glycogen storage disease XIII; 612932; ENO3 Glycogen storage disease XIV; 612934; PGM1 Glycogen storage disease XV; 613507;

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

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