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:0060321 | umbilical hernia | |
DOID:0060327 | omphalocele | |
DOID:0060467 | humeroradial synostosis | |
DOID:0060538 | purpura fulminans | |
DOID:0060575 | 3MC syndrome 1 | |
DOID:0060576 | 3MC syndrome 2 | |
DOID:0060577 | 3MC syndrome 3 | |
DOID:0080073 | spina bifida occulta | |
DOID:0080301 | atypical hemolytic-uremic syndrome | |
DOID:0080348 | Alzheimer's disease 1 |
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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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024