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:5844 | myocardial infarction | |
DOID:5854 | silent myocardial infarction | |
DOID:6682 | spondylolisthesis | |
DOID:6713 | cerebrovascular disease | |
DOID:674 | cleft palate | |
DOID:7148 | rheumatoid arthritis | |
DOID:758 | situs inversus | |
DOID:848 | arthritis | |
DOID:8725 | vascular dementia | |
DOID:8857 | lupus erythematosus |
HPO ID | HPO Term |
---|---|
HP:0002678 | Skull asymmetry |
HP:0002714 | Downturned corners of mouth |
HP:0002825 | Caudal appendage |
HP:0002827 | Hip dislocation |
HP:0002974 | Radioulnar synostosis |
HP:0003298 | Spina bifida occulta |
HP:0003307 | Hyperlordosis |
HP:0004209 | Clinodactyly of the 5th finger |
HP:0004298 | Abnormality of the abdominal wall |
HP:0004440 | Coronal craniosynostosis |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:257920 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105470889 | MACNE16135 | ||
101017684 | PAPAN24166 | ||
105527857 | MANLE32144 | ||
101144543 | GORGO27859 | ||
100970830 | PANPA29480 | ||
100439814 | PONAB25475 | ||
488121 | CANLF13568 | ||
112926302 | VULVU20581 | ||
123801287 | URSAM23233 | ||
101674101 | MUSPF16510 |
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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