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:0110048 | Alzheimer's disease 15 | |
DOID:0110106 | atrial heart septal defect 1 | |
DOID:0110107 | atrial heart septal defect 2 | |
DOID:0110108 | atrial heart septal defect 3 | |
DOID:0110109 | atrial heart septal defect 4 | |
DOID:0110110 | atrial heart septal defect 5 | |
DOID:0110111 | atrial heart septal defect 6 | |
DOID:0110112 | atrial heart septal defect 7 | |
DOID:0110113 | atrial heart septal defect 8 | |
DOID:0110114 | atrial heart septal defect 9 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000126 | Hydronephrosis |
HP:0000175 | Cleft palate |
HP:0000202 | Orofacial cleft |
HP:0000204 | Cleft upper lip |
HP:0000252 | Microcephaly |
HP:0000260 | Wide anterior fontanel |
HP:0000316 | Hypertelorism |
HP:0000365 | Hearing impairment |
HP:0000369 | Low-set ears |
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