GO Term |
---|
extracellular region |
plasma membrane |
collagen-containing extracellular matrix |
endoplasmic reticulum lumen |
Golgi lumen |
cell surface |
side of membrane |
lysosomal lumen |
GO Term |
---|
peptidyl-dipeptidase inhibitor activity |
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:0110109 | atrial heart septal defect 4 | |
DOID:0110110 | atrial heart septal defect 5 | |
DOID:0110111 | atrial heart septal defect 6 | |
DOID:0110112 | atrial heart septal defect 7 | |
DOID:0110113 | atrial heart septal defect 8 | |
DOID:0110114 | atrial heart septal defect 9 | |
DOID:0110213 | isolated cleft palate | |
DOID:0111029 | hemochromatosis type 1 | |
DOID:0111135 | congenital generalized lipodystrophy type 1 | |
DOID:0111136 | congenital generalized lipodystrophy type 2 |
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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