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 |
---|---|
HS-GAG degradation | Homo sapiens |
Post-translational protein phosphorylation | Homo sapiens |
RSV-host interactions | Homo sapiens |
Regulation of IGF Activity by IGFBP | Homo sapiens |
Respiratory syncytial virus (RSV) attachment and entry | Homo sapiens |
Retinoid metabolism and transport | Homo sapiens |
Syndecan interactions | Homo sapiens |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060190 | ileocolitis | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060270 | pontocerebellar hypoplasia type 2D | |
DOID:0060276 | pontocerebellar hypoplasia type 7 | |
DOID:0060277 | pontocerebellar hypoplasia type 8 | |
DOID:0060278 | pontocerebellar hypoplasia type 9 | |
DOID:0060469 | Miller-Dieker lissencephaly syndrome | |
DOID:0060807 | syndromic X-linked intellectual disability Najm type | |
DOID:0070027 | CST3-related cerebral amyloid angiopathy | |
DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 |
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