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
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Transmembrane topology of human glucose 6-phosphate transporter.
Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype.
The catalytic center of glucose-6-phosphatase. HIS176 is the nucleophile forming the phosphohistidine-enzyme intermediate during catalysis.
Glycogen storage disease type Ia in Argentina: two novel glucose-6-phosphatase mutations affecting protein stability.
Brain contains a functional glucose-6-phosphatase complex capable of endogenous glucose production.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a.
Glycogen storage disease type 1a in Israel: biochemical, clinical, and mutational studies.
Transmembrane topology of glucose-6-phosphatase.
Defective G6PC does not hydrolyze glucose 6-phosphate
G6PC hydrolyzes G6P to Glc and Pi (liver)
TCF19:NuRD represses G6PC gene expression