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:0110048 | Alzheimer's disease 15 | |
DOID:0110106 | atrial heart septal defect 1 | |
DOID:0110107 | atrial heart septal defect 2 | |
DOID:0110108 | atrial heart septal defect 3 | |
DOID:0110109 | atrial heart septal defect 4 | |
DOID:0110110 | atrial heart septal defect 5 | |
DOID:0110111 | atrial heart septal defect 6 | |
DOID:0110112 | atrial heart septal defect 7 | |
DOID:0110113 | atrial heart septal defect 8 | |
DOID:0110114 | atrial heart septal defect 9 |
HPO ID | HPO Term |
---|---|
HP:0004443 | Lambdoidal craniosynostosis |
HP:0005105 | Abnormal nasal morphology |
HP:0006216 | Single interphalangeal crease of fifth finger |
HP:0006394 | Limited pronation/supination of forearm |
HP:0008689 | Bilateral cryptorchidism |
HP:0008897 | Postnatal growth retardation |
HP:0009237 | Short 5th finger |
HP:0009891 | Underdeveloped supraorbital ridges |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:257920 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100038300 | Xenbase:XB-GENE-984453 | ||
101942804 | CHRPI11561 | ||
109308542 | CROPO15376 | ||
100551064 | MELGA02751 | ||
103815377 | SERCA08976 | ||
100082252 | ORNAN25025 | ||
100407253 | CALJA11916 | ||
105575210 | CERAT15715 | ||
101866962 | MACFA25802 | ||
708206 | MACMU29120 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024