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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
transaldolase 1
Summary
- Gene Symbol
-
- TALDO1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative initiation
- Cytoplasm
- Disease variant
- Nucleus
- Pentose shunt
- Phosphoprotein
- Reference proteome
- Schiff base
- Transferase
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A140VK56 |
|
| P37837 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fructose 6-phosphate metabolic process | ||
| pentose-phosphate shunt, non-oxidative branch | ||
| carbohydrate metabolic process |
GO Hierarchy
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| monosaccharide binding | ||
| protein binding | ||
| transaldolase activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Uncharacterized protein
- Functional Category
-
- G: Carbohydrate transport and metabolism
- J: Translation, ribosomal structure and biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| pentose-phosphate shunt, non-oxidative branch |
| pentose-phosphate shunt |
| transaldolase activity |
| transferase activity |
| InterPro |
|---|
| Aldolase-type TIM barrel |
| Transaldolase type 1 |
| Transaldolase, active site |
| Transaldolase/Fructose-6-phosphate aldolase |
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:2978 | carbohydrate metabolic disorder |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000056 | Abnormal clitoris morphology |
| HP:0000077 | Abnormality of the kidney |
| HP:0000154 | Wide mouth |
| HP:0000233 | Thin vermilion border |
| HP:0000260 | Wide anterior fontanel |
| HP:0000322 | Short philtrum |
| HP:0000325 | Triangular face |
| HP:0000369 | Low-set ears |
| HP:0000470 | Short neck |
| Disease ID | Disease Name |
|---|---|
| OMIM:606003 |
|
| ORPHA:101028 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 100657121 | LOXAF00717 | |||
| 100689344 | CRIGR19736 | |||
| 100701115 | ORENI33232 | |||
| 100718064 | CAVPO24826 | |||
| 100773203 | CRIGR19736 | |||
| 100855463 | CANLF20452 | |||
| 100922508 | SARHA13564 | |||
| 100994858 | 9597_0:002eeb | PANPA05840 | ||
| 101083034 | FELCA24118 | |||
| 101142562 | 9595_0:0036a3 | GORGO02709 |
