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:14261 | fragile X syndrome | |
DOID:1432 | blindness | |
DOID:14320 | generalized anxiety disorder | |
DOID:1443 | cerebral degeneration | |
DOID:14525 | Reye syndrome | |
DOID:14557 | primary pulmonary hypertension | |
DOID:14681 | Silver-Russell syndrome | |
DOID:14796 | Dubowitz syndrome | |
DOID:1485 | cystic fibrosis | |
DOID:150 | disease of mental health |
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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