GO Term | Evidence Code | PMID |
---|---|---|
mitochondrial citrate transmembrane transport | ||
fatty-acyl-CoA biosynthetic process | ||
gluconeogenesis |
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
mitochondrial inner membrane | ||
mitochondrion | ||
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
citrate secondary active transmembrane transporter activity | ||
antiporter activity | ||
citrate transmembrane transporter activity | ||
tricarboxylic acid transmembrane transporter activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050573 | 2-hydroxyglutaric aciduria | |
DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | |
DOID:0111619 | combined D-2- and L-2-hydroxyglutaric aciduria | |
DOID:11198 | DiGeorge syndrome | |
DOID:3635 | congenital myasthenic syndrome | |
DOID:700 | mitochondrial metabolism disease |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100726986 | CAVPO03167 | ||
101573407 | OCTDE05747 | ||
101723635 | HETGA17338 | ||
102458241 | PELSI04703 | ||
107086057 | CYPVA08901 | ||
107089647 | CYPVA13313 | ||
114041151 | VOMUR28384 | ||
113907202 | BOBOX32760 | ||
100956977 | OTOGA01931 | ||
112148868 | ORYME11514 |
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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