GO Term |
---|
focal adhesion |
lysosomal lumen |
Position | Description | PubMed ID | GlyTouCan ID | Source |
---|---|---|---|---|
28 |
|
|||
40 |
|
|||
42 | O-linked (GalNAc...) threonine | |||
49 |
|
|||
52 |
|
|
||
65 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
71 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
76 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
89 | N-linked (GlcNAc...) asparagine |
|
||
210 |
|
|
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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Last updated: August 19, 2024