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:10974 | oophoritis | |
DOID:0001816 | angiosarcoma | |
DOID:0002116 | pterygium | |
DOID:0014667 | disease of metabolism | |
DOID:0040085 | bacterial sepsis | |
DOID:0050012 | chikungunya | |
DOID:0050156 | idiopathic pulmonary fibrosis | |
DOID:0050328 | congenital hypothyroidism | |
DOID:0050387 | nonpapillary renal cell carcinoma | |
DOID:0050424 | familial adenomatous polyposis |
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 |
---|---|---|---|
101934126 | CHRPI32780 | ||
109314456 | CROPO20698 | ||
113446168 | PSETE19273 | ||
103820781 | SERCA17468 | ||
100074273 | ORNAN21342 | ||
100398849 | CALJA42099 | ||
105580892 | CERAT29002 | ||
102143464 | MACFA23596 | ||
710552 | MACMU22126 | ||
105478978 | MACNE37776 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024