GO Term | Evidence Code | PMID |
---|---|---|
regulation of angiogenesis | ||
endocytosis | ||
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction | ||
neutrophil chemotaxis |
|
|
mast cell degranulation |
|
GO Term | Evidence Code | PMID |
---|---|---|
kinase activity | ||
ephrin receptor binding | ||
1-phosphatidylinositol-3-kinase activity | ||
protein serine/threonine kinase activity | ||
protein serine kinase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050424 | familial adenomatous polyposis | |
DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | |
DOID:0050452 | mevalonic aciduria | |
DOID:0050457 | Sertoli cell-only syndrome | |
DOID:0050458 | juvenile myelomonocytic leukemia | |
DOID:0050469 | Costello syndrome | |
DOID:0050486 | exanthem | |
DOID:0050523 | adult T-cell leukemia/lymphoma | |
DOID:0050535 | exudative vitreoretinopathy | |
DOID:0050569 | Seckel syndrome |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000010 | Recurrent urinary tract infections |
HP:0000403 | Recurrent otitis media |
HP:0000964 | Eczematoid dermatitis |
HP:0001252 | Hypotonia |
HP:0001433 | Hepatosplenomegaly |
HP:0001581 | Recurrent skin infections |
HP:0001742 | Nasal congestion |
HP:0001744 | Splenomegaly |
HP:0001873 | Thrombocytopenia |
Disease ID | Disease Name |
---|---|
OMIM:619802 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
113436774 | PSETE01002 | ||
103813517 | SERCA06309 | ||
100078046 | ORNAN05315 | ||
100925455 | SARHA13743 | ||
103118136 | ERIEU07700 | ||
100394268 | CALJA43660 | ||
105583147 | CERAT13725 | ||
698857 | MACMU32743 | ||
105475319 | MACNE00055 | ||
101018542 | PAPAN30844 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024