GO Term |
---|
cell migration |
dendrite morphogenesis |
regulation of dendrite morphogenesis |
GO Term |
---|
endoplasmic reticulum lumen |
Golgi lumen |
cell surface |
lysosomal lumen |
plasma membrane |
collagen-containing extracellular matrix |
GO Term |
---|
PDZ domain binding |
identical protein binding |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
41 | O-linked (Xyl...) (glycosaminoglycan) serine |
|
||
55 | O-linked (Xyl...) (glycosaminoglycan) serine |
|
||
57 | O-linked (Xyl...) (glycosaminoglycan) serine |
|
||
74 |
|
|||
77 |
|
|||
80 |
|
|||
81 |
|
|||
86 |
|
|||
88 |
|
|||
89 |
|
Pathway Name | Organism |
---|---|
A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
Attachment and Entry | Homo sapiens |
Cell surface interactions at the vascular wall | 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 EXT1 causes exostoses 1, TRPS2 and CHDS | Homo sapiens |
Defective EXT2 causes exostoses 2 | Homo sapiens |
EPHB-mediated forward signaling | Homo sapiens |
HS-GAG 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:0050453 | lissencephaly | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050777 | Joubert syndrome | |
DOID:0050788 | proximal symphalangism | |
DOID:0050819 | obsolete Matthew-Wood syndrome | |
DOID:0050865 | tongue squamous cell carcinoma | |
DOID:0050894 | ameloblastoma | |
DOID:0060180 | colitis | |
DOID:0060189 | ileitis |
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