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PMID:5643703

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Citation

Beutler, E, Mathai, CK and Smith, JE (1968) Biochemical variants of glucose-6-phosphate dehydrogenase giving rise to congenital nonspherocytic hemolytic disease. Blood 31:131-50

Abstract

No abstract in PubMed

Links

PubMed

Keywords

Adolescent; Adult; Anemia, Hemolytic, Congenital; Child; Child, Preschool; Chromium Isotopes; Electrophoresis; Female; Glucosephosphate Dehydrogenase/analysis; Glucosephosphate Dehydrogenase Deficiency; Humans; Male; Molecular Biology; Mutation; Spectrophotometry

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

HUMAN:G6PD

enables

GO:0004345: glucose-6-phosphate dehydrogenase activity

ECO:0000315: mutant phenotype evidence used in manual assertion

F

Seeded From UniProt

complete

HUMAN:G6PD

enables

GO:0005536: glucose binding

ECO:0000315: mutant phenotype evidence used in manual assertion

F

Seeded From UniProt

complete

HUMAN:G6PD

involved_in

GO:0019322: pentose biosynthetic process

ECO:0000314: direct assay evidence used in manual assertion

P

Seeded From UniProt

complete

HUMAN:G6PD

involved_in

GO:0043249: erythrocyte maturation

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

HUMAN:G6PD

involved_in

GO:0051156: glucose 6-phosphate metabolic process

ECO:0000315: mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete


See also

References

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