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:0002678 | Skull asymmetry |
HP:0002714 | Downturned corners of mouth |
HP:0002825 | Caudal appendage |
HP:0002827 | Hip dislocation |
HP:0002974 | Radioulnar synostosis |
HP:0003298 | Spina bifida occulta |
HP:0003307 | Hyperlordosis |
HP:0004209 | Clinodactyly of the 5th finger |
HP:0004298 | Abnormality of the abdominal wall |
HP:0004440 | Coronal craniosynostosis |
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