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:0060321 | umbilical hernia | |
DOID:0060327 | omphalocele | |
DOID:0060467 | humeroradial synostosis | |
DOID:0060538 | purpura fulminans | |
DOID:0060575 | 3MC syndrome 1 | |
DOID:0060576 | 3MC syndrome 2 | |
DOID:0060577 | 3MC syndrome 3 | |
DOID:0080073 | spina bifida occulta | |
DOID:0080301 | atypical hemolytic-uremic syndrome | |
DOID:0080348 | Alzheimer's disease 1 |
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