GO Term | Evidence Code | PMID |
---|---|---|
actin cytoskeleton organization | ||
cell migration | ||
T cell receptor signaling pathway | ||
positive regulation of protein localization to membrane | ||
response to leucine |
GO Term | Evidence Code | PMID |
---|---|---|
kinase activity | ||
1-phosphatidylinositol-3-kinase activity | ||
insulin receptor substrate binding | ||
protein serine/threonine kinase activity | ||
protein serine kinase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050746 | mantle cell lymphoma | |
DOID:0050747 | obsolete lymphoplasmacytic lymphoma | |
DOID:0050749 | peripheral T-cell lymphoma | |
DOID:0050753 | cerebellar ataxia | |
DOID:0050757 | deafness-dystonia-optic neuronopathy syndrome | |
DOID:0050759 | myotonic dystrophy type 2 | |
DOID:0050765 | neuroacanthocytosis | |
DOID:0050766 | choreaacanthocytosis | |
DOID:0050771 | pheochromocytoma | |
DOID:0050778 | Meckel syndrome |
HPO ID | HPO Term |
---|---|
HP:0100780 | Conjunctival hamartoma |
HP:0100790 | Hernia |
HP:0100835 | Benign neoplasm of the central nervous system |
HP:0200008 | Intestinal polyposis |
HP:0200034 | Papule |
HP:0200063 | Colorectal polyposis |
Disease ID | Disease Name |
---|---|
OMIM:615108 |
|
OMIM:613659 |
|
ORPHA:276280 |
|
OMIM:612918 |
|
OMIM:619538 |
|
ORPHA:221061 |
|
ORPHA:201 |
|
ORPHA:60040 |
|
OMIM:114550 |
|
OMIM:182000 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101004976 | PAPAN25259 | ||
105539923 | MANLE14159 | ||
101143811 | GORGO29508 | ||
100990828 | PANPA29285 | ||
460858 | PANTR32684 | ||
100453779 | PONAB25917 | ||
488084 | CANLF13490 | ||
112926217 | VULVU20440 | ||
123786407 | URSAM12723 | ||
100479294 | AILME19605 |
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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