Gene Ontology annotation through association of InterPro records with GO terms

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

Combined Automated Annotation using Multiple IEA Methods

Phosphoglucomutase 1: complete human and rabbit mRNA sequences and direct mapping of this highly polymorphic marker on human chromosome 1.

Regulation of phosphoglucomutase 1 phosphorylation and activity by a signaling kinase.

Large-scale proteomics and phosphoproteomics of urinary exosomes.

Genome-wide YFP fluorescence complementation screen identifies new regulators for telomere signaling in human cells.

In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.

Compromised catalysis and potential folding defects in in vitro studies of missense mutants associated with hereditary phosphoglucomutase 1 deficiency.

Induced Structural Disorder as a Molecular Mechanism for Enzyme Dysfunction in Phosphoglucomutase 1 Deficiency.

Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency.

The Metabolic Map into the Pathomechanism and Treatment of PGM1-CDG.

Phosphoglucomutase 1: a gene with two promoters and a duplicated first exon.

Defective PGM1 does not isomerise G6P to G1P

Exocytosis of tertiary granule lumen proteins

Exocytosis of ficolin-rich granule lumen proteins

PGM1:Mg2+ isomerises G1P to G6P

PGM1:Mg2+ isomerises G6P to G1P