GO Term |
---|
synapse organization |
circulatory system development |
negative regulation of angiogenesis |
animal organ regeneration |
response to hypoxia |
receptor-mediated endocytosis |
response to xenobiotic stimulus |
smoothened signaling pathway |
GO Term |
---|
extracellular region |
basement membrane |
extracellular space |
plasma membrane |
axon |
Golgi lumen |
focal adhesion |
lysosomal lumen |
collagen-containing extracellular matrix |
plasma membrane protein complex |
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:0110213 | isolated cleft palate | |
DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | |
DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A | |
DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | |
DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | |
DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | |
DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | |
DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | |
DOID:0110281 | autosomal recessive limb-girdle muscular dystrophy type 2G |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024