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 |
---|---|---|---|
176398 | WB:WBGene00010780 | ||
189611 | WB:WBGene00021345 | ||
3772221 | FB:FBgn0037912 | ||
100176157 | CIOIN10889 | ||
103183998 | CALMI28709 | ||
102351464 | LATCH17535 | ||
793282 | ZFIN:ZDB-GENE-081104-41 | DANRE43021 | |
795332 | ZFIN:ZDB-GENE-130114-1 | DANRE01487 | |
393579 | ZFIN:ZDB-GENE-040426-1172 | ||
100528216 | ICTPU09194 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024