AAH42677.1
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
NCBI Official Full Name
H6pd protein
NCBI Official Synonym Full Names
hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
NCBI Protein Information
GDH/6PGL endoplasmic bifunctional protein; glucose 1-dehydrogenase; glucose-6-phosphate dehydrogenase 1
UniProt Protein Name
GDH/6PGL endoplasmic bifunctional protein
UniProt Synonym Protein Names
Hexose-6-phosphate dehydrogenase
UniProt Synonym Gene Names
UniProt Entry Name
G6PE_MOUSE
UniProt Comments for H6pd
H6PD: Oxidizes glucose-6-phosphate and glucose, as well as other hexose-6-phosphates. Defects in H6PD are a cause of cortisone reductase deficiency (CRD). In CRD, activation of cortisone to cortisol does not occur, resulting in adrenocorticotropin-mediated androgen excess and a phenotype resembling polycystic ovary syndrome (PCOS).
Protein type: EC 3.1.1.31; Oxidoreductase; Hydrolase; Carbohydrate Metabolism - pentose phosphate pathway; EC 1.1.1.47
Cellular Component: mitochondrion; intracellular membrane-bound organelle; endoplasmic reticulum; cytoplasm
Molecular Function: glucose-6-phosphate dehydrogenase activity; hydrolase activity; 6-phosphogluconolactonase activity; oxidoreductase activity; glucose 1-dehydrogenase activity; carbohydrate binding; NADP binding; catalytic activity
Biological Process: pentose-phosphate shunt; metabolic process; carbohydrate metabolic process; glucose metabolic process; NADP metabolic process
Research Articles on H6pd
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Pathways associated with anti-H6pd antibody
Diseases associated with anti-H6pd antibody
Organs/Tissues associated with anti-H6pd antibody
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