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:1059 | intellectual disability | |
DOID:10952 | nephritis | |
DOID:11247 | disseminated intravascular coagulation | |
DOID:11383 | cryptorchidism | |
DOID:12140 | Chagas disease | |
DOID:12305 | Bloch-Sulzberger syndrome | |
DOID:1289 | neurodegenerative disease | |
DOID:1394 | urinary schistosomiasis | |
DOID:1395 | schistosomiasis | |
DOID:13994 | cleidocranial dysplasia |
HPO ID | HPO Term |
---|---|
HP:0000506 | Telecanthus |
HP:0000508 | Ptosis |
HP:0000537 | Epicanthus inversus |
HP:0000581 | Blepharophimosis |
HP:0000593 | Abnormal anterior chamber morphology |
HP:0000925 | Abnormality of the vertebral column |
HP:0001249 | Intellectual disability |
HP:0001263 | Global developmental delay |
HP:0001363 | Craniosynostosis |
HP:0001382 | Joint hypermobility |
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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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