GO Term |
---|
embryonic hindlimb morphogenesis |
regulation of canonical Wnt signaling pathway |
negative regulation of canonical Wnt signaling pathway |
positive regulation of canonical Wnt signaling pathway |
GO Term |
---|
endoplasmic reticulum lumen |
Golgi lumen |
cell surface |
extracellular region |
plasma membrane |
collagen-containing extracellular matrix |
side of membrane |
lysosomal lumen |
GO Term |
---|
peptidyl-dipeptidase inhibitor activity |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
124 | N-linked (GlcNAc...) asparagine | |||
241 | N-linked (GlcNAc...) asparagine | |||
359 |
|
|||
418 | N-linked (GlcNAc...) asparagine |
|
||
495 | O-linked (Xyl...) (glycosaminoglycan) serine |
|
||
509 | O-linked (Xyl...) (glycosaminoglycan) serine |
|
||
|
Pathway Name | Organism |
---|---|
A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
Attachment and Entry | 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 |
HS-GAG biosynthesis | Homo sapiens |
HS-GAG degradation | Homo sapiens |
Post-translational protein phosphorylation | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
DOID:6873 | skin tag | |
DOID:688 | embryonal cancer | |
DOID:758 | situs inversus | |
DOID:769 | neuroblastoma | |
DOID:8398 | osteoarthritis | |
DOID:848 | arthritis | |
DOID:8488 | polyhydramnios | |
DOID:8923 | skin melanoma | |
DOID:8927 | learning disability | |
DOID:898 | autosomal dominant polycystic kidney disease |
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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