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:1074 | kidney failure | |
DOID:10871 | age related macular degeneration | |
DOID:10907 | microcephaly | |
DOID:10952 | nephritis | |
DOID:11111 | hydronephrosis | |
DOID:11247 | disseminated intravascular coagulation | |
DOID:11383 | cryptorchidism | |
DOID:114 | heart disease | |
DOID:11847 | coronary thrombosis | |
DOID:11870 | Pick's disease |
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 |
---|---|---|---|
100774526 | CRIGR00914 | ||
17174 | MGI:88492 | MOUSE19135 | |
64023 | RGD:620213 | RATNO03703 | |
100730575 | CAVPO04369 | ||
101571926 | OCTDE19382 | ||
101872767 | MELUD15699 | ||
100012016 | MONDO31913 | ||
103676043 | URSMA08560 | ||
113890940 | BOBOX29448 | ||
102025802 | CHILA06023 |
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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