Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Combined Automated Annotation using Multiple IEA Methods
Histidine 167 is the phosphate acceptor in glucose-6-phosphatase-beta forming a phosphohistidine enzyme intermediate during catalysis.
Defining the membrane proteome of NK cells.
Functional analysis of mutations in a severe congenital neutropenia syndrome caused by glucose-6-phosphatase-β deficiency.
G6PC3 hydrolyzes G6P to form Glc and Pi (ubiquitous)
Defective G6PC3 does not hydrolyze glucose 6-phosphate
Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency.
Biochemical characterization of the human ubiquitous glucose-6-phosphatase in neutrophil granulocytes.
Brain contains a functional glucose-6-phosphatase complex capable of endogenous glucose production.
Gluconeogenesis in developing rat kidney cortex.
Identification and characterization of a human cDNA and gene encoding a ubiquitously expressed glucose-6-phosphatase catalytic subunit-related protein.
A syndrome with congenital neutropenia and mutations in G6PC3.
Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia.