UniProt | Protein Name |
---|---|
O00329 |
|
A0A2K8FKV1 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of neutrophil apoptotic process | ||
T cell differentiation | ||
B cell differentiation |
|
|
B cell activation |
|
|
adaptive immune response |
|
GO Term | Evidence Code | PMID |
---|---|---|
kinase activity | ||
1-phosphatidylinositol-3-kinase activity | ||
1-phosphatidylinositol-4-phosphate 3-kinase activity | ||
1-phosphatidylinositol-4,5-bisphosphate 3-kinase activity | ||
ATP binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | |
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 | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050589 | inflammatory bowel disease |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000010 | Recurrent urinary tract infections |
HP:0000086 | Ectopic kidney |
HP:0000122 | Unilateral renal agenesis |
HP:0000252 | Microcephaly |
HP:0000306 | Abnormality of the chin |
HP:0000316 | Hypertelorism |
HP:0000348 | High forehead |
HP:0000365 | Hearing impairment |
Disease ID | Disease Name |
---|---|
OMIM:613328 |
|
OMIM:615513 |
|
OMIM:619281 |
|
ORPHA:221139 |
|
ORPHA:397596 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
174762 | WB:WBGene00000090 | ||
42446 | FB:FBgn0015279 | ||
103184230 | CALMI29388 | ||
394174 | ZFIN:ZDB-GENE-040426-1128 | DANRE25405 | |
108276156 | ICTPU07992 | ||
113581289 | ELEEL28038 | ||
106572046 | SALSA42822 | ||
115165908 | SALTR87491 | ||
115554025 | GADMO28278 | ||
101161887 | ORYLA15642 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024