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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

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. In humans there

Enolase

Alpha-enolase

Protein-coding gene in Homo sapiens

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

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

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

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

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 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