GO Term | Evidence Code | PMID |
---|---|---|
glycerol catabolic process | ||
canonical glycolysis | ||
glyceraldehyde-3-phosphate biosynthetic process | ||
glycolytic process | ||
methylglyoxal biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
protein homodimerization activity | ||
triose-phosphate isomerase activity | ||
ubiquitin protein ligase binding | ||
methylglyoxal synthase activity | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050486 | exanthem | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050700 | cardiomyopathy | |
DOID:0050757 | deafness-dystonia-optic neuronopathy syndrome | |
DOID:0050865 | tongue squamous cell carcinoma | |
DOID:0050884 | triosephosphate isomerase deficiency | |
DOID:0060041 | autism spectrum disorder | |
DOID:0080199 | colorectal carcinoma | |
DOID:0080326 | familial hypertrophic cardiomyopathy |
HPO ID | HPO Term |
---|---|
HP:0001878 | Hemolytic anemia |
HP:0001895 | Normochromic anemia |
HP:0001897 | Normocytic anemia |
HP:0001972 | Macrocytic anemia |
HP:0002059 | Cerebral atrophy |
HP:0002093 | Respiratory insufficiency |
HP:0002098 | Respiratory distress |
HP:0002317 | Unsteady gait |
HP:0002747 | Respiratory insufficiency due to muscle weakness |
HP:0002808 | Kyphosis |
Disease ID | Disease Name |
---|---|
ORPHA:868 |
|
OMIM:615512 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100052671 | HORSE37544 | ||
100157582 | PIGXX26291 | ||
102168433 | CAPHI25532 | ||
100348316 | RABIT12326 | ||
21991 | MGI:98797 | ||
24849 | RGD:3896 | ||
500959 | RGD:1560534 | ||
102452390 | PELSI06567 | ||
100565792 | ANOCA13659 | ||
114028957 | VOMUR31008 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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