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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
citrate synthase
Summary
- Gene Symbol
-
- CS
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Direct protein sequencing
- Methylation
- Mitochondrion
- Reference proteome
- Transferase
- Transit peptide
- Tricarboxylic acid cycle
- Ubl conjugation
- Proteins
| UniProt | Protein Name |
|---|---|
| O75390 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| carbohydrate metabolic process | ||
| citrate metabolic process | ||
| tricarboxylic acid cycle |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| mitochondrial matrix | ||
| mitochondrion | ||
| extracellular exosome |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| citrate (Si)-synthase activity | ||
| RNA binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:11254 | Brill-Zinsser disease | |
| DOID:0040085 | bacterial sepsis | |
| DOID:3083 | chronic obstructive pulmonary disease | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0050771 | pheochromocytoma | |
| DOID:0050782 | Zollinger-Ellison syndrome | |
| DOID:0050830 | peripheral artery disease | |
| DOID:0050852 | limb ischemia | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060235 | carnitine palmitoyltransferase II deficiency |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115150430 | SALTR32171 | ||
| 115165660 | SALTR86058 | ||
| 115168001 | SALTR73938 | ||
| 115540903 | GADMO27339 | ||
| 101155930 | ORYLA16110 | ||
| 100708317 | ORENI36337 | ||
| 115585052 | SPAAU51624 | ||
| 379886 | Xenbase:XB-GENE-943167 | ||
| 108709827 | Xenbase:XB-GENE-17333218 | ||
| 550067 | Xenbase:XB-GENE-943160 |
