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:0000007 | Autosomal recessive inheritance |
HP:0000543 | Optic disc pallor |
HP:0000762 | Decreased nerve conduction velocity |
HP:0000952 | Jaundice |
HP:0001081 | Cholelithiasis |
HP:0001082 | Cholecystitis |
HP:0001252 | Hypotonia |
HP:0001257 | Spasticity |
HP:0001263 | Global developmental delay |
HP:0001265 | Hyporeflexia |
Disease ID | Disease Name |
---|---|
ORPHA:868 |
|
OMIM:615512 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115176542 | SALTR43219 | ||
115177273 | SALTR85673 | ||
100049499 | ORYLA05875 | ||
380168 | Xenbase:XB-GENE-866354 | ||
108696046 | Xenbase:XB-GENE-17342467 | ||
100038162 | Xenbase:XB-GENE-494465 | ||
101939241 | CHRPI26463 | ||
109319388 | CROPO06478 | ||
113444550 | PSETE17179 | ||
100915433 | SARHA04974 |
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