UniProt | Protein Name |
---|---|
Q9BWP8 |
|
GO Term | Evidence Code | PMID |
---|---|---|
complement activation, lectin pathway | ||
cell surface pattern recognition receptor signaling pathway |
|
|
developmental process | ||
proteolysis | ||
complement activation |
GO Term | Evidence Code | PMID |
---|---|---|
collagen trimer | ||
extracellular region |
|
|
external side of plasma membrane |
|
|
serine-type endopeptidase complex |
|
|
extracellular space |
GO Term | Evidence Code | PMID |
---|---|---|
calcium ion binding | ||
protein binding | ||
identical protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0040085 | bacterial sepsis | |
DOID:0050597 | intestinal schistosomiasis | |
DOID:0060225 | 3MC syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060260 | ptosis | |
DOID:0060261 | congenital ptosis | |
DOID:0060321 | umbilical hernia | |
DOID:0060327 | omphalocele | |
DOID:0060467 | humeroradial synostosis | |
DOID:0060538 | purpura fulminans |
HPO ID | HPO Term |
---|---|
HP:0002974 | Radioulnar synostosis |
HP:0002996 | Limited elbow movement |
HP:0003298 | Spina bifida occulta |
HP:0003307 | Hyperlordosis |
HP:0003468 | Abnormal vertebral morphology |
HP:0003577 | Congenital onset |
HP:0005105 | Abnormal nasal morphology |
HP:0005243 | Partial abdominal muscle agenesis |
HP:0006394 | Limited pronation/supination of forearm |
HP:0008689 | Bilateral cryptorchidism |
Disease ID | Disease Name |
---|---|
ORPHA:293843 |
|
OMIM:265050 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
743061 | PANTR26993 | ||
100438992 | PONAB22538 | ||
482958 | CANLF04853 | ||
123786607 | URSAM27857 | ||
117802068 | AILME02384 | ||
101670087 | MUSPF16252 | ||
101091014 | FELCA06300 | ||
122216658 | PANLE01558 | ||
101339949 | TURTR05351 | ||
118906050 | BALMU05578 |
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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