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:0110760 | type 1 diabetes mellitus 23 | |
DOID:0110761 | type 1 diabetes mellitus 24 | |
DOID:0110844 | xeroderma pigmentosum group C | |
DOID:0110858 | polycystic kidney disease 1 | |
DOID:0110892 | inflammatory bowel disease 1 | |
DOID:0110910 | leukocyte adhesion deficiency 1 | |
DOID:0111005 | cone-rod dystrophy 2 | |
DOID:0111029 | hemochromatosis type 1 | |
DOID:0111135 | congenital generalized lipodystrophy type 1 | |
DOID:0111136 | congenital generalized lipodystrophy type 2 |
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 |
---|---|---|---|
115036690 | ECHNA41811 | ||
115403926 | SALFA10000 | ||
113490925 | ATHCN05581 | ||
105815179 | PROCO05914 | ||
109060929 | CYPCA63285 | ||
109064199 | CYPCA33330 | ||
103732179 | NANGA02072 | ||
116442892 | CORMO19998 | ||
103252973 | CARSF17749 | ||
115605592 | STRHB21515 |
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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