GO Term | Evidence Code | PMID |
---|---|---|
regulation of insulin secretion | ||
regulation of glycolytic process | ||
glucose catabolic process | ||
intracellular glucose homeostasis | ||
glucose 6-phosphate metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
cytosol | ||
mitochondrion | ||
nucleoplasm |
GO Term | Evidence Code | PMID |
---|---|---|
glucose sensor activity | ||
glucose binding | ||
glucokinase activity | ||
ATP binding | ||
mannokinase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:8947 | diabetic retinopathy | |
DOID:9065 | leishmaniasis | |
DOID:9074 | systemic lupus erythematosus | |
DOID:9146 | visceral leishmaniasis | |
DOID:9267 | urea cycle disorder | |
DOID:9351 | diabetes mellitus | |
DOID:9352 | type 2 diabetes mellitus | |
DOID:9452 | steatotic liver disease | |
DOID:9521 | Laron syndrome | |
DOID:9588 | encephalitis |
HPO ID | HPO Term |
---|---|
HP:0008255 | Transient neonatal diabetes mellitus |
HP:0008283 | Fasting hyperinsulinemia |
HP:0010864 | Intellectual disability, severe |
HP:0010935 | Abnormality of the upper urinary tract |
HP:0011106 | Hypovolemia |
HP:0011462 | Young adult onset |
HP:0012028 | Hepatocellular adenoma |
HP:0012378 | Fatigue |
HP:0012594 | Moderate albuminuria |
HP:0012638 | Abnormal nervous system physiology |
Disease ID | Disease Name |
---|---|
OMIM:602485 |
|
ORPHA:552 |
|
OMIM:606176 |
|
ORPHA:79299 |
|
ORPHA:99885 |
|
OMIM:125851 |
|
OMIM:125853 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
850317 | SGD:S000000545 | ||
850614 | SGD:S000001949 | ||
852128 | SGD:S000002924 | ||
852639 | SGD:S000003222 | ||
109100787 | CYPCA73357 | ||
103734982 | NANGA09168 | ||
116435523 | CORMO13063 | ||
115618479 | STRHB19498 |
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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