GO Term |
---|
interphotoreceptor matrix |
lysosomal lumen |
perineuronal net |
extracellular region |
extracellular space |
membrane |
extracellular matrix |
synapse |
collagen-containing extracellular matrix |
photoreceptor outer segment |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
51 |
|
|||
57 | N-linked (GlcNAc...) asparagine | |||
330 | N-linked (GlcNAc...) asparagine |
|
||
362 |
|
|||
364 |
|
|||
393 |
|
|||
440 |
|
|||
442 |
|
|||
464 |
|
|||
471 |
|
Pathway Name | Organism |
---|---|
A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
CS/DS degradation | Homo sapiens |
Chondroitin sulfate biosynthesis | Homo sapiens |
Defective B3GALT6 causes EDSP2 and SEMDJL1 | Homo sapiens |
Defective B3GAT3 causes JDSSDHD | Homo sapiens |
Defective B4GALT7 causes EDS, progeroid type | Homo sapiens |
Defective CHST14 causes EDS, musculocontractural type | Homo sapiens |
Defective CHST3 causes SEDCJD | Homo sapiens |
Defective CHSY1 causes TPBS | Homo sapiens |
Dermatan sulfate biosynthesis | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050156 | idiopathic pulmonary fibrosis | |
DOID:0050387 | nonpapillary renal cell carcinoma | |
DOID:0050469 | Costello syndrome | |
DOID:0050589 | inflammatory bowel disease | |
DOID:0050801 | androgenic alopecia | |
DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | |
DOID:0050819 | obsolete Matthew-Wood syndrome | |
DOID:0050902 | medulloblastoma | |
DOID:0060247 | Smith-McCort dysplasia | |
DOID:0080199 | colorectal carcinoma |
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