GO Term |
---|
plasma membrane |
axon |
Pathway Name | Organism |
---|---|
A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
Amyloid fiber formation | 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 |
Degradation of the extracellular matrix | Homo sapiens |
ECM proteoglycans | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
DOID:4658 | benign mastocytoma | |
DOID:3183 | childhood oligodendroglioma | |
DOID:3186 | adult oligodendroglioma | |
DOID:3312 | bipolar disorder | |
DOID:3355 | fibrosarcoma | |
DOID:3371 | chondrosarcoma | |
DOID:3393 | coronary artery disease | |
DOID:3490 | Noonan syndrome | |
DOID:350 | mastocytosis | |
DOID:3516 | adult fibrosarcoma |
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