GO Term |
---|
neuronal cell body |
extracellular exosome |
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:10348 | blepharophimosis | |
DOID:1040 | chronic lymphocytic leukemia | |
DOID:10588 | adrenoleukodystrophy | |
DOID:10591 | pre-eclampsia | |
DOID:1063 | interstitial nephritis | |
DOID:10652 | Alzheimer's disease | |
DOID:1074 | kidney failure | |
DOID:10871 | age related macular degeneration | |
DOID:10907 | microcephaly | |
DOID:1094 | attention deficit hyperactivity disorder |
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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