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:12217 | Lewy body dementia | |
DOID:12305 | Bloch-Sulzberger syndrome | |
DOID:12554 | hemolytic-uremic syndrome | |
DOID:1287 | cardiovascular system disease | |
DOID:13515 | tuberous sclerosis | |
DOID:13620 | patent foramen ovale | |
DOID:13832 | patent ductus arteriosus | |
DOID:13994 | cleidocranial dysplasia | |
DOID:1432 | blindness | |
DOID:14323 | Marfan syndrome |
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 |
---|---|---|---|
105729900 | AOTNA33595 | ||
110210181 | PHACI13766 | ||
101033147 | SAIBB11872 | ||
111216830 | SERDU16817 | ||
108433970 | PYGNA17673 | ||
101969600 | ICTTR07070 | ||
103152966 | POEFO18428 | ||
102427812 | MYOLU02451 | ||
117032206 | RHIFE06300 | ||
100231782 | TAEGU30129 |
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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