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 |
---|---|---|
phosphatidylinositol 3-kinase complex | ||
lamellipodium | ||
intercalated disc | ||
perinuclear region of cytoplasm |
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:8947 | diabetic retinopathy | |
DOID:898 | autosomal dominant polycystic kidney disease | |
DOID:8991 | cervix uteri carcinoma in situ | |
DOID:8997 | polycythemia vera | |
DOID:90 | degenerative disc disease | |
DOID:9007 | sudden infant death syndrome | |
DOID:9008 | psoriatic arthritis | |
DOID:9065 | leishmaniasis | |
DOID:9074 | systemic lupus erythematosus | |
DOID:9080 | macroglobulinemia |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000020 | Urinary incontinence |
HP:0000034 | Hydrocele testis |
HP:0000036 | Abnormal penis morphology |
HP:0000044 | Hypogonadotropic hypogonadism |
HP:0000077 | Abnormality of the kidney |
HP:0000089 | Renal hypoplasia |
HP:0000098 | Tall stature |
HP:0000105 | Enlarged kidney |
HP:0000130 | Abnormality of the uterus |
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 |
---|---|---|---|
103479066 | POERE11713 | ||
102304410 | HAPBU21841 | ||
113010568 | ASTCA16628 | ||
115572921 | SPAAU36085 | ||
373752 | Xenbase:XB-GENE-998109 | ||
108718090 | Xenbase:XB-GENE-17344667 | ||
100144924 | Xenbase:XB-GENE-998106 | ||
101935421 | CHRPI14535 | ||
109308275 | CROPO15200 | ||
113439753 | PSETE11548 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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