GO Term | Evidence Code | PMID |
---|---|---|
ERAD pathway | ||
oligosaccharide metabolic process | ||
viral protein processing | ||
mannose trimming involved in glycoprotein ERAD pathway | ||
mannoprotein catabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
endosome |
|
|
endoplasmic reticulum | ||
trans-Golgi network |
|
|
endoplasmic reticulum quality control compartment | ||
endoplasmic reticulum membrane |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050429 | Hailey-Hailey disease | |
DOID:0050454 | periventricular nodular heterotopia | |
DOID:0050570 | congenital disorder of glycosylation type I | |
DOID:0050889 | non-syndromic intellectual disability | |
DOID:0060262 | gallbladder disease | |
DOID:0060762 | restrictive dermopathy | |
DOID:0060810 | syndromic X-linked intellectual disability type 10 | |
DOID:0060823 | syndromic X-linked intellectual disability 94 | |
DOID:0060862 | mal de Meleda | |
DOID:0070129 | autosomal recessive cutis laxa type IID |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000219 | Thin upper lip vermilion |
HP:0000256 | Macrocephaly |
HP:0000268 | Dolichocephaly |
HP:0000272 | Malar flattening |
HP:0000276 | Long face |
HP:0000286 | Epicanthus |
HP:0000307 | Pointed chin |
HP:0000316 | Hypertelorism |
HP:0000319 | Smooth philtrum |
Disease ID | Disease Name |
---|---|
OMIM:614202 |
|
ORPHA:397941 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
177726 | WB:WBGene00013881 | ||
180787 | WB:WBGene00020197 | ||
43436 | FB:FBgn0039634 | ||
103180403 | CALMI20321 | ||
556237 | ZFIN:ZDB-GENE-070705-482 | DANRE36389 | |
562592 | ZFIN:ZDB-GENE-091116-34 | ||
103022471 | ASTMX14339 | ||
108255760 | ICTPU17080 | ||
113577930 | ELEEL20988 | ||
106579997 | SALSA95346 |
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
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: August 19, 2024