GO Term | Evidence Code | PMID |
---|---|---|
Golgi organization | ||
protein transport | ||
retrograde transport, vesicle recycling within Golgi | ||
intra-Golgi vesicle-mediated transport | ||
glycosylation |
GO Term | Evidence Code | PMID |
---|---|---|
trans-Golgi network membrane |
|
|
Golgi membrane | ||
Golgi transport complex | ||
Golgi stack |
GO Term | Evidence Code | PMID |
---|---|---|
protein binding | ||
protein-containing complex binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0060224 | atrial fibrillation | |
DOID:0070269 | congenital disorder of glycosylation type IIq | |
DOID:10534 | stomach cancer | |
DOID:114 | heart disease | |
DOID:11832 | visual epilepsy | |
DOID:12697 | locked-in syndrome | |
DOID:12835 | quadriplegia | |
DOID:1287 | cardiovascular system disease | |
DOID:13810 | familial hypercholesterolemia | |
DOID:1390 | hypobetalipoproteinemia |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0001249 | Intellectual disability |
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001410 | Decreased liver function |
HP:0001999 | Abnormal facial shape |
HP:0002079 | Hypoplasia of the corpus callosum |
HP:0002361 | Psychomotor deterioration |
HP:0002506 | Diffuse cerebral atrophy |
HP:0002510 | Spastic tetraplegia |
Disease ID | Disease Name |
---|---|
ORPHA:435934 |
|
OMIM:617395 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
177473 | WB:WBGene00000585 | ||
41870 | FB:FBgn0026634 | ||
103186437 | CALMI34663 | ||
102363033 | LATCH14989 | ||
406663 | ZFIN:ZDB-GENE-040426-2671 | DANRE05470 | |
103037537 | ASTMX10934 | ||
113571499 | ELEEL10556 | ||
115152849 | SALTR08356 | ||
115201479 | SALTR100041 | ||
115559970 | GADMO14811 |
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