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:2590 | familial nephrotic syndrome | |
DOID:2730 | epidermolysis bullosa | |
DOID:2744 | pyelitis | |
DOID:2891 | thyroid adenoma | |
DOID:2914 | immune system disease | |
DOID:2921 | glomerulonephritis | |
DOID:2962 | Cockayne syndrome | |
DOID:2964 | periarthritis | |
DOID:2986 | IgA glomerulonephritis | |
DOID:305 | carcinoma |
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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