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
Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b.
Human variant glucose-6-phosphate transporter is active in microsomal transport.
The signature motif in human glucose-6-phosphate transporter is essential for microsomal transport of glucose-6-phosphate.
The glucose-6-phosphate transporter is a phosphate-linked antiporter deficient in glycogen storage disease type Ib and Ic.
Defining the membrane proteome of NK cells.
A new variant of glycogen storage disease type I probably due to a defect in the glucose-6-phosphate transport system.
SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters.
A reference map of the human binary protein interactome.
SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylation.
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.
Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib.
SLC7A4 exchanges G6P for Pi across the ER membrane
Defective SLC37A4 does not exchange G6P and Pi across the ER membrane