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:0060875 | isolated growth hormone deficiency type III | |
DOID:0070331 | mitochondrial DNA depletion syndrome 8b | |
DOID:0080119 | mitochondrial DNA depletion syndrome 1 | |
DOID:0080123 | mitochondrial DNA depletion syndrome 4b | |
DOID:0080124 | mitochondrial DNA depletion syndrome 5 | |
DOID:0080127 | mitochondrial DNA depletion syndrome 8a | |
DOID:0080177 | hepatic veno-occlusive disease | |
DOID:0080199 | colorectal carcinoma | |
DOID:0090070 | hypogonadotropic hypogonadism | |
DOID:0090071 | hypogonadotropic hypogonadism 11 with or without anosmia |
HPO ID | HPO Term |
---|---|
HP:0002500 | Abnormal cerebral white matter morphology |
HP:0002522 | Areflexia of lower limbs |
HP:0002578 | Gastroparesis |
HP:0002579 | Gastrointestinal dysmotility |
HP:0002910 | Elevated circulating hepatic transaminase concentration |
HP:0002922 | Increased CSF protein concentration |
HP:0002936 | Distal sensory impairment |
HP:0003128 | Lactic acidosis |
HP:0003199 | Decreased muscle mass |
HP:0003200 | Ragged-red muscle fibers |
Disease ID | Disease Name |
---|---|
ORPHA:298 |
|
OMIM:603041 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
107580729 | SINGR11100 | ||
109532673 | HIPCM18983 | ||
115404023 | SALFA09174 | ||
103382511 | CYNSE28518 | ||
105813932 | PROCO21368 | ||
109094498 | CYPCA33391 | ||
103735486 | NANGA18165 |
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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