UniProt | Protein Name |
---|---|
Q9BWP8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
complement activation, lectin pathway | ||
cell surface pattern recognition receptor signaling pathway |
|
|
developmental process | ||
proteolysis | ||
complement activation |
GO Term | Evidence Code | PMID |
---|---|---|
collagen trimer | ||
extracellular region |
|
|
external side of plasma membrane |
|
|
serine-type endopeptidase complex |
|
|
extracellular space |
GO Term | Evidence Code | PMID |
---|---|---|
DNA binding | ||
oligosaccharide binding | ||
fucose binding | ||
calcium-dependent carbohydrate binding | ||
mannose binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:1425 | pyoureter | |
DOID:2340 | craniosynostosis | |
DOID:2527 | nephrosis | |
DOID:2921 | glomerulonephritis | |
DOID:3156 | hypomelanosis of Ito | |
DOID:399 | tuberculosis | |
DOID:526 | human immunodeficiency virus infectious disease | |
DOID:539 | ophthalmoplegia | |
DOID:540 | strabismus | |
DOID:552 | pneumonia |
HPO ID | HPO Term |
---|---|
HP:0002974 | Radioulnar synostosis |
HP:0002996 | Limited elbow movement |
HP:0003298 | Spina bifida occulta |
HP:0003307 | Hyperlordosis |
HP:0003468 | Abnormal vertebral morphology |
HP:0003577 | Congenital onset |
HP:0005105 | Abnormal nasal morphology |
HP:0005243 | Partial abdominal muscle agenesis |
HP:0006394 | Limited pronation/supination of forearm |
HP:0008689 | Bilateral cryptorchidism |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:265050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115035498 | ECHNA39637 | ||
115406706 | SALFA11402 | ||
105820466 | PROCO29318 | ||
109086045 | CYPCA100774 | ||
109107771 | CYPCA88568 | ||
103747645 | NANGA00383 | ||
116442002 | CORMO18450 | ||
115610018 | STRHB17178 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024