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:1443 | cerebral degeneration | |
DOID:14525 | Reye syndrome | |
DOID:1485 | cystic fibrosis | |
DOID:162 | cancer | |
DOID:1657 | ventricular septal defect | |
DOID:1686 | glaucoma | |
DOID:1749 | squamous cell carcinoma | |
DOID:1837 | diabetic ketoacidosis | |
DOID:1882 | atrial heart septal defect | |
DOID:1883 | hepatitis C |
HPO ID | HPO Term |
---|---|
HP:0001540 | Diastasis recti |
HP:0001629 | Ventricular septal defect |
HP:0001631 | Atrial septal defect |
HP:0001643 | Patent ductus arteriosus |
HP:0001769 | Broad foot |
HP:0001773 | Short foot |
HP:0002265 | Large fleshy ears |
HP:0002553 | Highly arched eyebrow |
HP:0002558 | Supernumerary nipple |
HP:0002650 | Scoliosis |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:257920 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100002060 | ZFIN:ZDB-GENE-110421-4 | ||
103022902 | ASTMX15544 | ||
108278363 | ICTPU10302 | ||
105008657 | ESOLU00556 | ||
115205811 | SALTR112983 | ||
115528837 | GADMO19034 | ||
103475256 | POERE07094 | ||
102289885 | HAPBU29455 | ||
398413 | Xenbase:XB-GENE-984458 | ||
398414 | Xenbase:XB-GENE-17335616 |
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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