GO Term | Evidence Code | PMID |
---|---|---|
regulation of angiogenesis | ||
endocytosis | ||
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction | ||
neutrophil chemotaxis |
|
|
mast cell degranulation |
|
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:14159 | obstructive hydrocephalus | |
DOID:14175 | von Hippel-Lindau disease | |
DOID:14177 | congenital hypogammaglobulinemia | |
DOID:14179 | X-linked agammaglobulinemia | |
DOID:14221 | abdominal obesity-metabolic syndrome 1 | |
DOID:14227 | azoospermia | |
DOID:1425 | pyoureter | |
DOID:14261 | fragile X syndrome | |
DOID:14291 | Noonan syndrome with multiple lentigines | |
DOID:14323 | Marfan syndrome |
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 |
---|---|---|---|
105544111 | MANLE13547 | ||
101153738 | GORGO39522 | ||
100988420 | PANPA36956 | ||
463649 | PANTR41142 | ||
100453085 | PONAB32940 | ||
483266 | CANLF05536 | ||
112908560 | VULVU34389 | ||
123789397 | URSAM07804 | ||
100470322 | AILME18428 | ||
101681462 | MUSPF19008 |
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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