GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of MAP kinase activity | ||
adaptive immune response |
|
|
sphingosine-1-phosphate receptor signaling pathway | ||
G protein-coupled receptor signaling pathway | ||
cell migration |
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:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0060901 | lymphoplasmacytic lymphoma | |
DOID:0070189 | X-linked spermatogenic failure 1 | |
DOID:0070314 | obstructive nephropathy | |
DOID:0070324 | systemic Epstein-Barr virus positive T-cell lymphoma of childhood | |
DOID:0070329 | mitochondrial DNA depletion syndrome | |
DOID:0080001 | bone disease | |
DOID:0080144 | childhood acute lymphocytic leukemia | |
DOID:0080145 | childhood T-cell acute lymphoblastic leukemia |
HPO ID | HPO Term |
---|---|
HP:0001880 | Eosinophilia |
HP:0001888 | Lymphopenia |
HP:0001890 | Autoimmune hemolytic anemia |
HP:0001904 | Neutropenia in presence of anti-neutropil antibodies |
HP:0001945 | Fever |
HP:0002014 | Diarrhea |
HP:0002027 | Abdominal pain |
HP:0002155 | Hypertriglyceridemia |
HP:0002583 | Colitis |
HP:0002716 | Lymphadenopathy |
Disease ID | Disease Name |
---|---|
OMIM:619802 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
115180047 | SALTR55207 | ||
115198746 | SALTR65231 | ||
115542827 | GADMO46053 | ||
101173828 | ORYLA10866 | ||
100697462 | ORENI23913 | ||
108711184 | Xenbase:XB-GENE-17340298 | ||
108713077 | Xenbase:XB-GENE-6487000 | ||
100158519 | Xenbase:XB-GENE-1011009 | ||
101948128 | CHRPI21551 | ||
109315724 | CROPO05404 |
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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