GO Term | Evidence Code | PMID |
---|---|---|
phospholipase C-activating G protein-coupled receptor signaling pathway | ||
phosphorylation | ||
negative regulation of triglyceride catabolic process | ||
dendritic cell chemotaxis |
|
|
phosphatidylinositol 3-kinase/protein kinase B signal transduction |
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:0060192 | Crohn's colitis | |
DOID:0060224 | atrial fibrillation | |
DOID:0060239 | Van der Woude syndrome | |
DOID:0060254 | Robinow syndrome | |
DOID:0060262 | gallbladder disease | |
DOID:0060306 | Meier-Gorlin syndrome | |
DOID:0060318 | acute promyelocytic leukemia | |
DOID:0060319 | cardiac arrest | |
DOID:0060389 | chromosome 10q23 deletion syndrome | |
DOID:0060448 | Fleck corneal dystrophy |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000010 | Recurrent urinary tract infections |
HP:0000403 | Recurrent otitis media |
HP:0000964 | Eczematoid dermatitis |
HP:0001252 | Hypotonia |
HP:0001433 | Hepatosplenomegaly |
HP:0001581 | Recurrent skin infections |
HP:0001742 | Nasal congestion |
HP:0001744 | Splenomegaly |
HP:0001873 | Thrombocytopenia |
Disease ID | Disease Name |
---|---|
OMIM:619802 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
113436774 | PSETE01002 | ||
103813517 | SERCA06309 | ||
100078046 | ORNAN05315 | ||
100925455 | SARHA13743 | ||
103118136 | ERIEU07700 | ||
100394268 | CALJA43660 | ||
105583147 | CERAT13725 | ||
698857 | MACMU32743 | ||
105475319 | MACNE00055 | ||
101018542 | PAPAN30844 |
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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