GO Term |
---|
collagen fibril organization |
transforming growth factor beta receptor complex assembly |
GO Term |
---|
extracellular region |
extracellular space |
extracellular matrix |
collagen-containing extracellular matrix |
Golgi lumen |
lysosomal lumen |
Pathway Name | Organism |
---|---|
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) | Homo sapiens |
Defective CHST6 causes MCDC1 | Homo sapiens |
Defective ST3GAL3 causes MCT12 and EIEE15 | Homo sapiens |
ECM proteoglycans | Homo sapiens |
Keratan sulfate biosynthesis | Homo sapiens |
Keratan sulfate degradation | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
DOID:2348 | arteriosclerotic cardiovascular disease | |
DOID:2349 | arteriosclerosis | |
DOID:2527 | nephrosis | |
DOID:2660 | cystic teratoma | |
DOID:2921 | glomerulonephritis | |
DOID:2964 | periarthritis | |
DOID:3068 | glioblastoma | |
DOID:3070 | high grade glioma | |
DOID:3071 | gliosarcoma | |
DOID:3074 | giant cell glioblastoma |
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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