GO Term | Evidence Code | PMID |
---|---|---|
phosphate ion transmembrane transport | ||
glucose metabolic process | ||
glucose homeostasis |
|
|
glucose-6-phosphate transport | ||
gluconeogenesis |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
endoplasmic reticulum membrane | ||
plasma membrane |
|
|
membrane |
GO Term | Evidence Code | PMID |
---|---|---|
glucose-6-phosphate transmembrane transporter activity | ||
glucose 6-phosphate:inorganic phosphate antiporter activity | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:6688 | autoimmune lymphoproliferative syndrome | |
DOID:684 | hepatocellular carcinoma | |
DOID:687 | hepatoblastoma | |
DOID:9007 | sudden infant death syndrome | |
DOID:9266 | cystinuria | |
DOID:9351 | diabetes mellitus | |
DOID:9352 | type 2 diabetes mellitus | |
DOID:9521 | Laron syndrome | |
DOID:9663 | aphthous stomatitis | |
DOID:9744 | type 1 diabetes mellitus |
HPO ID | HPO Term |
---|---|
HP:0001408 | Bile duct proliferation |
HP:0001508 | Failure to thrive |
HP:0001510 | Growth delay |
HP:0001538 | Protuberant abdomen |
HP:0001629 | Ventricular septal defect |
HP:0001636 | Tetralogy of Fallot |
HP:0001733 | Pancreatitis |
HP:0001744 | Splenomegaly |
HP:0001763 | Pes planus |
HP:0001873 | Thrombocytopenia |
Disease ID | Disease Name |
---|---|
OMIM:232240 |
|
OMIM:619525 |
|
ORPHA:79259 |
|
OMIM:232220 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101323404 | TURTR05954 | ||
118898987 | BALMU08163 | ||
100656239 | LOXAF06093 | ||
100063238 | HORSE39342 | ||
100516688 | PIGXX35554 | ||
506423 | BOVIN06584 | ||
102173104 | CAPHI06116 | ||
101105355 | SHEEP06153 | ||
100357958 | RABIT16786 | ||
105980834 | DIPOR02917 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024