GO Term | Evidence Code | PMID |
---|---|---|
angiogenesis | ||
regulation of transmission of nerve impulse | ||
chemotaxis | ||
pyrimidine nucleobase metabolic process | ||
regulation of gastric motility |
GO Term | Evidence Code | PMID |
---|---|---|
thymidine phosphorylase activity | ||
protein homodimerization activity | ||
growth factor activity | ||
protein binding | ||
pyrimidine-nucleoside phosphorylase activity |
|
DO ID | Disease Name | Source |
---|---|---|
DOID:655 | inherited metabolic disorder | |
DOID:657 | adenoma | |
DOID:6726 | fibrillary astrocytoma | |
DOID:6811 | juvenile pilocytic astrocytoma | |
DOID:684 | hepatocellular carcinoma | |
DOID:699 | mitochondrial myopathy | |
DOID:700 | mitochondrial metabolism disease | |
DOID:7005 | gemistocytic astrocytoma | |
DOID:7007 | childhood cerebral astrocytoma | |
DOID:7008 | protoplasmic astrocytoma |
HPO ID | HPO Term |
---|---|
HP:0007108 | Demyelinating peripheral neuropathy |
HP:0007141 | Sensorimotor neuropathy |
HP:0008049 | Abnormality of the extraocular muscles |
HP:0009027 | Foot dorsiflexor weakness |
HP:0009830 | Peripheral neuropathy |
HP:0011024 | Abnormality of the gastrointestinal tract |
HP:0012103 | Abnormality of the mitochondrion |
HP:0012533 | Allodynia |
HP:0012850 | Small intestinal dysmotility |
HP:0100613 | Death in early adulthood |
Disease ID | Disease Name |
---|---|
ORPHA:298 |
|
OMIM:603041 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115542459 | GADMO44961 | ||
115542463 | GADMO44961 | ||
101159551 | ORYLA11292 | ||
100699577 | ORENI25978 | ||
102308981 | HAPBU07374 | ||
115595786 | SPAAU48961 | ||
108710281 | Xenbase:XB-GENE-17335259 | ||
100145512 | Xenbase:XB-GENE-995988 | ||
101950024 | CHRPI22163 | ||
103164808 | ORNAN05738 |
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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