GO Term | Evidence Code | PMID |
---|---|---|
gluconeogenesis |
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:0001290 | Generalized hypotonia |
HP:0001324 | Muscle weakness |
HP:0001332 | Dystonia |
HP:0001337 | Tremor |
HP:0001508 | Failure to thrive |
HP:0001522 | Death in infancy |
HP:0001562 | Oligohydramnios |
HP:0001635 | Congestive heart failure |
HP:0001639 | Hypertrophic cardiomyopathy |
HP:0001744 | Splenomegaly |
Disease ID | Disease Name |
---|---|
ORPHA:868 |
|
OMIM:615512 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
114587774 | PODMU23882 | ||
107549487 | SINGR69888 | ||
106847322 | EQUAS05657 | ||
116837582 | CHEAB23298 | ||
105295948 | PTEVA01703 | ||
115044805 | ECHNA27493 | ||
115397033 | SALFA31673 | ||
851620 | SGD:S000002457 | ||
109048699 | CYPCA34698 | ||
109104501 | CYPCA60306 |
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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