UniProt | Protein Name |
---|---|
P48740 |
|
GO Term | Evidence Code | PMID |
---|---|---|
complement activation, lectin pathway | ||
zymogen activation |
GO Term | Evidence Code | PMID |
---|---|---|
cytosol | ||
extracellular region |
|
|
extracellular space | ||
nucleoplasm |
GO Term | Evidence Code | PMID |
---|---|---|
protein homodimerization activity | ||
peptidase activity | ||
serine-type endopeptidase activity | ||
calcium ion binding | ||
calcium-dependent protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:12217 | Lewy body dementia | |
DOID:12305 | Bloch-Sulzberger syndrome | |
DOID:12554 | hemolytic-uremic syndrome | |
DOID:1287 | cardiovascular system disease | |
DOID:13515 | tuberous sclerosis | |
DOID:13620 | patent foramen ovale | |
DOID:13832 | patent ductus arteriosus | |
DOID:13994 | cleidocranial dysplasia | |
DOID:1432 | blindness | |
DOID:14323 | Marfan syndrome |
HPO ID | HPO Term |
---|---|
HP:0000593 | Abnormal anterior chamber morphology |
HP:0000664 | Synophrys |
HP:0000678 | Dental crowding |
HP:0000960 | Sacral dimple |
HP:0001249 | Intellectual disability |
HP:0001256 | Intellectual disability, mild |
HP:0001363 | Craniosynostosis |
HP:0001510 | Growth delay |
HP:0001537 | Umbilical hernia |
HP:0001539 | Omphalocele |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:257920 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
108530465 | RHIBE00803 | ||
104653539 | RHIRO05729 | ||
100601109 | NOMLE02889 | ||
114598179 | PODMU37227 | ||
107582221 | SINGR27403 | ||
107586740 | SINGR10268 | ||
111573564 | AMPOC17910 | ||
106832546 | EQUAS17299 | ||
116823020 | CHEAB02192 | ||
115052730 | ECHNA07201 |
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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