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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
aconitase 2
Summary
- Gene Symbol
-
- ACO2
- Aliases
-
- ACONM
- aconitate hydratase, mitochondrial
- mitochondrial aconitase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 4Fe-4S
- Acetylation
- Direct protein sequencing
- Disease variant
- Lyase
- Mitochondrion
- Neurodegeneration
- Phosphoprotein
- Reference proteome
- Transit peptide
- Tricarboxylic acid cycle
- Proteins
| UniProt | Protein Name |
|---|---|
| Q99798 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol | ||
| mitochondrial matrix |
|
|
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| 4 iron, 4 sulfur cluster binding | ||
| 3 iron, 4 sulfur cluster binding | ||
| aconitate hydratase activity | ||
| iron ion 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:0110462 | autosomal recessive nonsyndromic deafness 101 | |
| DOID:0050564 | autosomal dominant nonsyndromic deafness | |
| DOID:0050565 | autosomal recessive nonsyndromic deafness | |
| DOID:0050566 | X-linked nonsyndromic deafness | |
| DOID:0050589 | inflammatory bowel disease | |
| DOID:0050883 | infantile cerebellar-retinal degeneration | |
| DOID:0060192 | Crohn's colitis | |
| DOID:0060690 | autosomal dominant auditory neuropathy 1 | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0060891 | Parkinson's disease 19A |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002305 | Athetosis |
| HP:0002500 | Abnormal cerebral white matter morphology |
| HP:0003593 | Infantile onset |
| HP:0003621 | Juvenile onset |
| HP:0004325 | Decreased body weight |
| HP:0007108 | Demyelinating peripheral neuropathy |
| HP:0007359 | Focal-onset seizure |
| HP:0007663 | Reduced visual acuity |
| HP:0010864 | Intellectual disability, severe |
| HP:0011344 | Severe global developmental delay |
| Disease ID | Disease Name |
|---|---|
| OMIM:614559 |
|
| OMIM:616289 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 176121 | WB:WBGene00000041 | ||
| 41326 | FB:FBgn0037862 | ||
| 44149 | FB:FBgn0010100 | ||
| 103189232 | CALMI40993 | ||
| 322670 | ZFIN:ZDB-GENE-030131-1390 | DANRE45736 | |
| 103029821 | ASTMX07738 | ||
| 103031515 | ASTMX14322 | ||
| 108273913 | ICTPU05126 | ||
| 113574872 | ELEEL17037 | ||
| 113584853 | ELEEL34038 |
