GO Term |
---|
plasma membrane |
axon |
Pathway Name | Organism |
---|---|
HS-GAG biosynthesis | Homo sapiens |
HS-GAG degradation | Homo sapiens |
Integrin cell surface interactions | Homo sapiens |
Laminin interactions | Homo sapiens |
Non-integrin membrane-ECM interactions | Homo sapiens |
RSV-host interactions | Homo sapiens |
Respiratory syncytial virus (RSV) attachment and entry | Homo sapiens |
Retinoid metabolism and transport | Homo sapiens |
DO ID | Disease Name | Source |
---|---|---|
DOID:1168 | familial hyperlipidemia | |
DOID:11714 | gestational diabetes | |
DOID:11719 | oculopharyngeal muscular dystrophy | |
DOID:11720 | distal myopathy | |
DOID:11722 | myotonic dystrophy type 1 | |
DOID:11723 | Duchenne muscular dystrophy | |
DOID:11724 | limb-girdle muscular dystrophy | |
DOID:11725 | Cornelia de Lange syndrome | |
DOID:11727 | facioscapulohumeral muscular dystrophy | |
DOID:11830 | myopia |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024